Canonical Allele Identifier: PA2828349268
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356506.1:p.Ala589Val
CA402528341
NM_001369577.1:c.1766C>T