Canonical Allele Identifier: PA2826200270
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 559301
ClinVar RCV Id: RCV000676806 RCV002532176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182181.2:p.Tyr111Cys
CA192400994
NM_001195252.2:c.332A>G