Canonical Allele Identifier: PA2825029061
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 1437568
ClinVar RCV Id: RCV001948763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000040.1:p.Arg233Gln
CA8289014
NM_000049.4:c.698G>A