HP c.998T>A ;(p.I333K)

Variant ID: 16-72094566-T-A

NM_005143.3(HP):c.998T>A;(p.I333K)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

A Supplement to TRANSFUSION Abstract Presentations from the AABB Annual Meeting Boston, MA, October 13-16, 2018.

Transfusion
Publication Date: 2018-10

Variant appearance in text: HP: 998T>A
PubMed Link: 30211950
Variant Present in the following documents:
  • Main text
View BVdb publication page