Canonical Allele Identifier: PA2827944922
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 574199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser1707Pro
CA16032519
NM_001354895.2:c.5119T>C