Allele Registry

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Canonical Allele Identifier: PA2826199806

Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 366594

ClinVar RCV Id: RCV000390070 RCV001844151 RCV002523789

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182177.2:p.Glu125Asp	CA10627234 NM_001195248.2:c.375A>T CA373179788 NM_001195248.2:c.375A>C