Allele Registry

Canonical Allele Identifier: PA357222

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000210647

ClinVar Variation:

224971

HGVS (amino-acid)	Matching Registered Transcripts
NP_000039.2:p.Glu86Ala	CA357221 NM_000048.4:c.257A>C