Canonical Allele Identifier: PA2826199820
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_001182177.2:p.Tyr183Cys
CA192400994
NM_001195248.2:c.548A>G