Canonical Allele Identifier: PA916061149
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 886
ClinVar RCV Id: RCV000000934 RCV000424623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_942002.1:p.His393Pro
CA114610
NM_198709.3:c.1178A>C