Canonical Allele Identifier: PA2573181925
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 1389126
ClinVar RCV Id: RCV001878147

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Cys311Arg
CA287021119
NM_001128085.1:c.931T>C