Canonical Allele Identifier: PA916041072
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470052

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2203Asn
CA045325
NM_001354896.2:c.6608G>A