Canonical Allele Identifier: PA2828352748
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356513.1:p.Arg551Trp
CA254160
NM_001369584.1:c.1651C>T