Allele Registry

Canonical Allele Identifier: PA091705

Gene: ASPA HGNC NCBI

ClinVar RCV:

RCV000169314

RCV001093138

RCV002265654

ClinVar Variation:

188940

HGVS (amino-acid)	Matching Registered Transcripts
NP_000040.1:p.Pro181Thr	CA274160 NM_000049.4:c.541C>A