Canonical Allele Identifier: PA658800731
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 445287
ClinVar RCV Id: RCV000656125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Ser94Leu
CA360196421
NM_000046.5:c.281C>T