Canonical Allele Identifier: PA2828353250
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356514.1:p.Arg551Trp
CA254160
NM_001369585.1:c.1651C>T