Allele Registry

Canonical Allele Identifier: PA915957137

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000493464

RCV000668710

ClinVar Variation:

288770

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Arg111Gln	CA4276905 NM_001024946.2:c.332G>A