Canonical Allele Identifier: PA645381191
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 266120
ClinVar RCV Id: RCV000256474
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Gln97Arg
CA10588994
NM_000046.5:c.290A>G