Canonical Allele Identifier: PA2825015930
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 572572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn627Ser
CA16025430
NM_000038.6:c.1880A>G