Allele Registry

Canonical Allele Identifier: PA2825338569

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000211672

ClinVar Variation:

226414

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020115.1:p.Met340Thr	CA10576340 NM_001024944.2:c.1019T>C