Allele Registry

Canonical Allele Identifier: PA357227

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000210677

ClinVar Variation:

224977

HGVS (amino-acid)	Matching Registered Transcripts
NP_000039.2:p.Arg297Trp	CA357226 NM_000048.4:c.889C>T