Canonical Allele Identifier: PA916061006
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_942002.1:p.Tyr210Cys
CA114609
NM_198709.3:c.629A>G