Canonical Allele Identifier: PA2827998871
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760090
ClinVar RCV Id: RCV002400466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro2500Leu
CA16038006
NM_001354901.2:c.7499C>T