Canonical Allele Identifier: PA2828013333
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 495374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp2496Gly
CA16038634
NM_001354905.2:c.7487A>G