Canonical Allele Identifier: PA2826321709
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230161.1:p.Arg509Trp
CA254160
NM_001243232.1:c.1525C>T