Canonical Allele Identifier: PA2828305479
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_001355935.1:p.Gly152Val
CA373176969
NM_001369006.1:c.455G>T