Canonical Allele Identifier: PA2826320777
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230159.1:p.Arg573Trp
CA254160
NM_001243230.2:c.1717C>T