Allele Registry

Canonical Allele Identifier: PA2825028707

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV003472630

ClinVar Variation:

2678634

HGVS (amino-acid)	Matching Registered Transcripts
NP_000039.2:p.Ala444Val	CA4277390 NM_000048.4:c.1331C>T