Canonical Allele Identifier: PA319961
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 214121
ClinVar RCV Id: RCV000195599 RCV003765258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_778243.1:p.Arg245His
CA319960
NM_175073.3:c.734G>A