Canonical Allele Identifier: PA2826321259
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230160.1:p.Arg534Trp
CA254160
NM_001243231.2:c.1600C>T