Canonical Allele Identifier: PA2580136673
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 1989078
ClinVar RCV Id: RCV002795484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Asn117Thr
CA397682312
NM_001128085.1:c.350A>C