Canonical Allele Identifier: PA2826199978
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 2242001
ClinVar RCV Id: RCV002724339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182178.1:p.Pro254Leu
CA5022333
NM_001195249.2:c.761C>T