Canonical Allele Identifier: PA091592
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 878
ClinVar RCV Id: RCV000000926 RCV000677550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Cys117Arg
CA114601
NM_000046.5:c.349T>C