Canonical Allele Identifier: PA091615
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Tyr210Cys
CA114609
NM_000046.5:c.629A>G