Canonical Allele Identifier: PA645381254
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 286086
ClinVar RCV Id: RCV000302376 RCV000401780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Asn458Ser
CA3317993
NM_000046.5:c.1373A>G