Canonical Allele Identifier: PA2826200295
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_001182181.2:p.Ser170Asn
CA321109
NM_001195252.2:c.509G>A