Canonical Allele Identifier: PA2827971610
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 922223
ClinVar RCV Id: RCV001182155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2552Pro
CA16038115
NM_001354898.2:c.7654T>C