Canonical Allele Identifier: PA2825027633
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 2153232

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Ala186Thr
CA121104198
NM_000046.5:c.556G>A