Canonical Allele Identifier: PA2827968805
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 661458
ClinVar RCV Id: RCV003537282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile1698Val
CA16032626
NM_001354898.2:c.5092A>G