Canonical Allele Identifier: PA645469819
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 381631
ClinVar RCV Id: RCV000432912 RCV001276652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Gly123Glu
CA16608396
NM_001128085.1:c.368G>A