Canonical Allele Identifier: PA916060871
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_942002.1:p.Arg95Gln
CA114608
NM_198709.3:c.284G>A