Allele Registry

Canonical Allele Identifier: PA658831388

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000413440

RCV000609637

ClinVar Variation:

372306

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020114.1:p.Arg193Gln	CA4277009 NM_001024943.2:c.578G>A