Allele Registry

Canonical Allele Identifier: PA091689

Gene: ASPA HGNC NCBI

ClinVar RCV:

RCV000002733

ClinVar Variation:

2615

HGVS (amino-acid)	Matching Registered Transcripts
NP_000040.1:p.Asp249Val	CA252364 NM_000049.4:c.746A>T