Allele Registry

Canonical Allele Identifier: PA658832063

Gene: ASPA HGNC NCBI

ClinVar RCV:

RCV000665070

RCV001844210

ClinVar Variation:

550346

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121557.1:p.Ile143Val	CA8288915 NM_001128085.1:c.427A>G