Canonical Allele Identifier: PA2828304351
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 286950
ClinVar RCV Id: RCV000351313
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355924.1:p.Arg318His
CA5022242
NM_001368995.1:c.953G>A