Canonical Allele Identifier: PA1139680440
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 929164
ClinVar RCV Id: RCV001194236 RCV001828602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Glu129Lys
CA8288909
NM_001128085.1:c.385G>A