Canonical Allele Identifier: PA2827968685
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile1665Val
CA040590
NM_001354898.2:c.4993A>G