Canonical Allele Identifier: PA115641
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 2616
ClinVar RCV Id: RCV000002734 RCV000363108 RCV001093136 RCV002415389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Arg71His
CA115640
NM_001128085.1:c.212G>A