Canonical Allele Identifier: PA2825638392
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 656514
ClinVar RCV Id: RCV003653381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Leu530Met
CA16024894
NM_001127511.3:c.1588T>A