Canonical Allele Identifier: PA2827998969
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2566989
ClinVar RCV Id: RCV003278282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.His2532Asn
CA16038212
NM_001354901.2:c.7594C>A