Canonical Allele Identifier: PA2827961897
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1445798
ClinVar RCV Id: RCV003745443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn2412Asp
CA16037019
NM_001354897.2:c.7234A>G