Allele Registry

Canonical Allele Identifier: PA2825028245

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000673369

ClinVar Variation:

557253

HGVS (amino-acid)	Matching Registered Transcripts
NP_000039.2:p.Asp87Gly	CA4276864 NM_000048.4:c.260A>G