Allele Registry

Canonical Allele Identifier: PA658825607

Gene: ARSB HGNC NCBI

ClinVar RCV:

RCV000677608

ClinVar Variation:

559825

HGVS (amino-acid)	Matching Registered Transcripts
NP_000037.2:p.Gly308Glu	CA360343477 NM_000046.5:c.923G>A