Canonical Allele Identifier: PA2827998333
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 188173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2339Phe
CA012909
NM_001354901.2:c.7016C>T