Allele Registry

Canonical Allele Identifier: PA916060791

Gene: ARSB HGNC NCBI

ClinVar RCV:

RCV000656127

ClinVar Variation:

445289

HGVS (amino-acid)	Matching Registered Transcripts
NP_942002.1:p.Leu51Pro	CA360196953 NM_198709.3:c.152T>C