Canonical Allele Identifier: PA2826200008
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 290957
ClinVar RCV Id: RCV000324352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182178.1:p.Pro330His
CA10606959
NM_001195249.2:c.989C>A