Canonical Allele Identifier: PA2827962178
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759033
ClinVar RCV Id: RCV002391439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro2499Thr
CA16037571
NM_001354897.2:c.7495C>A