Canonical Allele Identifier: PA2828011502
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 187494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn2217Ser
CA012867
NM_001354905.2:c.6650A>G