Canonical Allele Identifier: PA658832064
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 557614
ClinVar RCV Id: RCV000673780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Ile143Thr
CA8288917
NM_001128085.1:c.428T>C