Canonical Allele Identifier: PA658800725
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 445289
ClinVar RCV Id: RCV000656127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Leu51Pro
CA360196953
NM_000046.5:c.152T>C