Canonical Allele Identifier: PA2826321289
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230160.1:p.Ala568Val
CA402528341
NM_001243231.2:c.1703C>T