Canonical Allele Identifier: PA2826916729
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293137.1:p.Ala539Val
CA402528341
NM_001306208.1:c.1616C>T