Allele Registry

Canonical Allele Identifier: PA2825338652

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV003472630

ClinVar Variation:

2678634

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020115.1:p.Ala424Val	CA4277390 NM_001024944.2:c.1271C>T