Canonical Allele Identifier: PA109393
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003190.1:p.Arg576Trp
CA254160
NM_003199.3:c.1726C>T