Canonical Allele Identifier: PA2828048786
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 75619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro2496Leu
CA16038424
NM_001354904.2:c.7487C>T