Canonical Allele Identifier: PA091594
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 880
ClinVar RCV Id: RCV000000928 RCV000179701 RCV000723435 RCV000779751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Cys405Tyr
CA114603
NM_000046.5:c.1214G>A