Allele Registry

Canonical Allele Identifier: PA915957055

Gene: ASL HGNC NCBI

ClinVar Allele:

415109

ClinVar RCV:

RCV000489610

RCV001836830

ClinVar Variation:

426324

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020114.1:p.Gln326His	CA4277213 NM_001024943.2:c.978G>C CA367646723 NM_001024943.2:c.978G>T