Allele Registry

Canonical Allele Identifier: PA2580136740

Gene: ASPA HGNC NCBI

ClinVar RCV:

RCV003123384

RCV003475529

ClinVar Variation:

2429145

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121557.1:p.His244Leu	CA397686327 NM_001128085.1:c.731A>T