Canonical Allele Identifier: PA091701
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 557614
ClinVar RCV Id: RCV000673780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000040.1:p.Ile143Thr
CA8288917
NM_000049.4:c.428T>C