Canonical Allele Identifier: PA2827999223
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 851804
ClinVar RCV Id: RCV002240266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn2608Ser
CA16038710
NM_001354901.2:c.7823A>G