Canonical Allele Identifier: PA2825028926
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 1176650
ClinVar RCV Id: RCV001532290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000040.1:p.Asn121Asp
CA8288902
NM_000049.4:c.361A>G