Canonical Allele Identifier: PA2828350265
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 393171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356508.1:p.Leu584Pro
CA16608769
NM_001369579.1:c.1751T>C