Allele Registry

Canonical Allele Identifier: PA1139670268

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV001047877

RCV003422083

ClinVar Variation:

203626

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Arg146Trp	CA312345 NM_001024946.2:c.436C>T