Canonical Allele Identifier: PA091705
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 188940
ClinVar RCV Id: RCV000169314 RCV001093138 RCV002265654
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000040.1:p.Pro181Thr
CA274160
NM_000049.4:c.541C>A