Allele Registry

Canonical Allele Identifier: PA2825338441

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000185776

RCV000987893

ClinVar Variation:

203625

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020115.1:p.Thr131Met	CA312343 NM_001024944.2:c.392C>T