Canonical Allele Identifier: PA2826916700
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293137.1:p.Arg505Trp
CA254160
NM_001306208.1:c.1513C>T