Canonical Allele Identifier: PA2827998978
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 161205

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn2534Ser
CA014033
NM_001354901.2:c.7601A>G