Allele Registry

Canonical Allele Identifier: PA091630

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV001047877

RCV003422083

ClinVar Variation:

203626

HGVS (amino-acid)	Matching Registered Transcripts
NP_000039.2:p.Arg146Trp	CA312345 NM_000048.4:c.436C>T