Canonical Allele Identifier: PA2828304920
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 2136752
ClinVar RCV Id: RCV003037319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355929.1:p.Ser188Asn
CA321109
NM_001369000.1:c.563G>A