Canonical Allele Identifier: PA2827992477
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 924397
ClinVar RCV Id: RCV001185687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn543Ile
CA16025271
NM_001354901.2:c.1628A>T