Canonical Allele Identifier: PA2827980538
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3071382
ClinVar RCV Id: RCV004015876

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala2473Asp
CA16037646
NM_001354899.2:c.7418C>A