Allele Registry

Canonical Allele Identifier: PA915957121

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000210603

RCV000489282

ClinVar Variation:

224970

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Glu59Lys	CA357215 NM_001024946.2:c.175G>A