Canonical Allele Identifier: PA2825638389
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Leu530Val
CA16024895
NM_001127511.3:c.1588T>G