Allele Registry

Canonical Allele Identifier: PA915957127

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000673369

ClinVar Variation:

557253

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Asp87Gly	CA4276864 NM_001024946.2:c.260A>G