Canonical Allele Identifier: PA658800730
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 445290
ClinVar RCV Id: RCV000656128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Leu82Arg
CA360196597
NM_000046.5:c.245T>G