Allele Registry

Canonical Allele Identifier: PA2825338837

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000210677

ClinVar Variation:

224977

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Arg271Trp	CA357226 NM_001024946.2:c.811C>T