Canonical Allele Identifier: PA2828023034
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Val1540Met
CA040215
NM_001354903.2:c.4618G>A