Canonical Allele Identifier: PA2827971546
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1015134
ClinVar RCV Id: RCV002242228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2532Pro
CA16037991
NM_001354898.2:c.7594T>C