Canonical Allele Identifier: PA2827947664
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133514
ClinVar RCV Id: RCV000120020 RCV000565915 RCV000589511 RCV003650377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ile2541Val
CA013946
NM_001354895.2:c.7621A>G