Canonical Allele Identifier: PA2828304319
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_001355924.1:p.Ser242Asn
CA321109
NM_001368995.1:c.725G>A