Canonical Allele Identifier: PA2828013384
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 851804
ClinVar RCV Id: RCV002240266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn2507Ser
CA16038710
NM_001354905.2:c.7520A>G