Allele Registry

Canonical Allele Identifier: PA645381253

Gene: ARSB HGNC NCBI

ClinVar RCV:

RCV000435336

RCV000632186

ClinVar Variation:

379809

HGVS (amino-acid)	Matching Registered Transcripts
NP_000037.2:p.Thr442Met	CA16604916 NM_000046.5:c.1325C>T