Canonical Allele Identifier: PA2828345725
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356499.1:p.Ala613Val
CA402528341
NM_001369570.1:c.1838C>T