Allele Registry

Canonical Allele Identifier: PA2825338027

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000210603

RCV000489282

ClinVar Variation:

224970

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020114.1:p.Glu59Lys	CA357215 NM_001024943.2:c.175G>A