Canonical Allele Identifier: PA2827989170
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2907983
ClinVar RCV Id: RCV003651671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly2329Asp
CA16036812
NM_001354900.2:c.6986G>A