Canonical Allele Identifier: PA2828353280
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356514.1:p.Ala585Val
CA402528341
NM_001369585.1:c.1754C>T