Canonical Allele Identifier: PA2827965279
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1783048
ClinVar RCV Id: RCV002413175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ala622Gly
CA16025556
NM_001354898.2:c.1865C>G