Canonical Allele Identifier: PA2825027649
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 1469785
ClinVar RCV Id: RCV001961748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Tyr210His
CA3318219
NM_000046.5:c.628T>C