Canonical Allele Identifier: PA2826916722
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 393171
ClinVar RCV Id: RCV000418798 RCV001507045
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293137.1:p.Leu534Pro
CA16608769
NM_001306208.1:c.1601T>C