Canonical Allele Identifier: PA2828019584
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Val832Met
CA035105
NM_001354906.2:c.2494G>A