Canonical Allele Identifier: PA2828352779
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356513.1:p.Ala585Val
CA402528341
NM_001369584.1:c.1754C>T