Canonical Allele Identifier: PA2827999084
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1052468
ClinVar RCV Id: RCV003771065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2568Ala
CA16038452
NM_001354901.2:c.7702T>G