Canonical Allele Identifier: PA2580134569
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1719864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn999Ser
CA16028012
NM_001127511.3:c.2996A>G