Canonical Allele Identifier: PA2827432130
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335143.1:p.Ala449Val
CA402528341
NM_001348214.2:c.1346C>T