Canonical Allele Identifier: PA2825645093
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn2725Ser
CA050243
NM_001127511.3:c.8174A>G