IDUA c.493+2T>C

Variant ID: 4-994779-T-C

NM_000203.3(IDUA):c.493+2T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.

Ebiomedicine
Foley, Samantha B SB; Rios, Jonathan J JJ; Mgbemena, Victoria E VE; Robinson, Linda S LS; Hampel, Heather L HL; Toland, Amanda E AE; Durham, Leslie L; Ross, Theodora S TS
Publication Date: 2015-01

Variant appearance in text: IDUA: 493+2T>C
PubMed Link: 26023681
Variant Present in the following documents:
  • mmc1.pdf
View BVdb publication page