Canonical Allele Identifier: PA2825028920
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 1989078
ClinVar RCV Id: RCV002795484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000040.1:p.Asn117Thr
CA397682312
NM_000049.4:c.350A>C