Canonical Allele Identifier: PA2826916301
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293136.1:p.Ala586Val
CA402528341
NM_001306207.1:c.1757C>T