Allele Registry

Canonical Allele Identifier: PA645469844

Gene: ASPA HGNC NCBI

ClinVar RCV:

RCV000411129

RCV003330657

ClinVar Variation:

371086

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121557.1:p.His244Arg	CA16041827 NM_001128085.1:c.731A>G