Canonical Allele Identifier: PA2825016105
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn660Ser
CA16025642
NM_000038.6:c.1979A>G