Canonical Allele Identifier: PA2580231159
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727379
ClinVar RCV Id: RCV002319894

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser987Gly
CA16028082
NM_001354900.2:c.2959A>G