Canonical Allele Identifier: PA2828344674
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356497.1:p.Arg580Trp
CA254160
NM_001369568.1:c.1738C>T