Canonical Allele Identifier: PA114607
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 883
ClinVar RCV Id: RCV000224599 RCV000677514 RCV000779750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Leu72Gln
CA114606
NM_000046.5:c.215T>A