Canonical Allele Identifier: PA2828000691
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1478972
ClinVar RCV Id: RCV002579516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His561Pro
CA16025590
NM_001354902.2:c.1682A>C