Canonical Allele Identifier: PA2827998855
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2496Ala
CA16037981
NM_001354901.2:c.7486T>G