Allele Registry

Canonical Allele Identifier: PA2825338972

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV003472630

ClinVar Variation:

2678634

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020117.1:p.Ala418Val	CA4277390 NM_001024946.2:c.1253C>T