Canonical Allele Identifier: PA916040510
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 638969
ClinVar RCV Id: RCV003653322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser1714Gly
CA16032450
NM_001354896.2:c.5140A>G