Canonical Allele Identifier: PA2828304958
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_001355929.1:p.Pro276His
CA10606959
NM_001369000.1:c.827C>A