Canonical Allele Identifier: PA091588
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 445292
ClinVar RCV Id: RCV000656130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Arg160Gln
CA360193893
NM_000046.5:c.479G>A