Canonical Allele Identifier: PA2828022844
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Val1358Met
CA040215
NM_001354906.2:c.4072G>A