Allele Registry

Canonical Allele Identifier: PA645469821

Gene: ASPA HGNC NCBI

ClinVar Allele:

360237

ClinVar RCV:

RCV000414045

RCV000675094

ClinVar Variation:

372307

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121557.1:p.Ile143Phe	CA8288916 NM_001128085.1:c.427A>T