Canonical Allele Identifier: PA2826200209
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 1807152
ClinVar RCV Id: RCV002475109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182180.1:p.Gly240Val
CA373176969
NM_001195251.2:c.719G>T