Canonical Allele Identifier: PA109323
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003190.1:p.Ala610Val
CA402528341
NM_003199.3:c.1829C>T