Allele Registry

Canonical Allele Identifier: PA2825338466

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000210597

ClinVar Variation:

224973

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020115.1:p.Leu154Pro	CA357213 NM_001024944.2:c.461T>C