Canonical Allele Identifier: PA916061017
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 879
ClinVar RCV Id: RCV000000927 RCV000677586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_942002.1:p.Leu236Pro
CA114602
NM_198709.3:c.707T>C