Allele Registry

Canonical Allele Identifier: PA145649

Gene: ARSB HGNC NCBI

ClinVar RCV:

RCV000077997

RCV000352809

RCV000675205

ClinVar Variation:

92350

HGVS (amino-acid)	Matching Registered Transcripts
NP_000037.2:p.Val358Met	CA145648 NM_000046.5:c.1072G>A