Canonical Allele Identifier: PA658825573
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 559779
ClinVar RCV Id: RCV000677558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Tyr138Cys
CA360194145
NM_000046.5:c.413A>G