Canonical Allele Identifier: PA2825015579
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Leu548Val
CA16024895
NM_000038.6:c.1642T>G