ERMAP c.1064C>T ;(p.P355L)

Variant ID: 1-43308539-C-T

NM_001017922.1(ERMAP):c.1064C>T;(p.P355L)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Using whole-genome sequencing to characterize clinically significant blood groups among healthy older Australians.

Blood Advances
Jadhao, Sudhir S; Davison, Candice C; Roulis, Eileen V EV; Lee, Simon S; Lacaze, Paul P; Riaz, Moeen M; McNeil, John J JJ; Thomas, David M DM; Pecheniuk, Natalie M NM; Hyland, Catherine A CA; Flower, Robert L RL; Nagaraj, Shivashankar H SH
Publication Date: 2022-08-09

Variant appearance in text: ERMAP: P355L; rs370816316
PubMed Link: 35420653
Variant Present in the following documents:
  • mmc1.xlsx, sheet 5
View BVdb publication page