Canonical Allele Identifier: PA2828352278
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356512.1:p.Ala586Val
CA402528341
NM_001369583.1:c.1757C>T