Allele Registry

Canonical Allele Identifier: PA915957060

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000002504

RCV000185769

ClinVar Variation:

2403

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020114.1:p.Arg379Cys	CA252265 NM_001024943.2:c.1135C>T