Canonical Allele Identifier: PA2827980828
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2566989
ClinVar RCV Id: RCV003278282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.His2563Asn
CA16038212
NM_001354899.2:c.7687C>A