Allele Registry

Canonical Allele Identifier: PA2573177172

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV001892645

ClinVar Variation:

1383503

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020114.1:p.Ala398Asp	CA312333 NM_001024943.2:c.1193C>A