Canonical Allele Identifier: PA2827999085
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 939073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2568Phe
CA049365
NM_001354901.2:c.7703C>T