Canonical Allele Identifier: PA658655206
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 444656
ClinVar RCV Id: RCV000512720 RCV001248198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Asp375Asn
CA3318117
NM_000046.5:c.1123G>A