Allele Registry

Canonical Allele Identifier: PA658655206

Gene: ARSB HGNC NCBI

ClinVar RCV:

RCV000512720

RCV001248198

ClinVar Variation:

444656

HGVS (amino-acid)	Matching Registered Transcripts
NP_000037.2:p.Asp375Asn	CA3318117 NM_000046.5:c.1123G>A