Canonical Allele Identifier: PA2825021117
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val1641Met
CA040215
NM_000038.6:c.4921G>A