Canonical Allele Identifier: PA2826323298
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230165.1:p.Ala450Val
CA402528341
NM_001243236.2:c.1349C>T