Allele Registry

Canonical Allele Identifier: PA915957128

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000178026

RCV000790828

ClinVar Variation:

92359

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Arg94Cys	CA220290 NM_001024946.2:c.280C>T