Allele Registry

Canonical Allele Identifier: PA658800725

Gene: ARSB HGNC NCBI

ClinVar RCV:

RCV000656127

ClinVar Variation:

445289

HGVS (amino-acid)	Matching Registered Transcripts
NP_000037.2:p.Leu51Pro	CA360196953 NM_000046.5:c.152T>C