Canonical Allele Identifier: PA2827335940
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317534.1:p.Ala484Val
CA402528341
NM_001330605.3:c.1451C>T