Canonical Allele Identifier: PA2828351600
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1722322
ClinVar RCV Id: RCV002302436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356511.1:p.Arg365Leu
CA402533894
NM_001369582.1:c.1094G>T