Canonical Allele Identifier: PA091683
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 2607
ClinVar RCV Id: RCV000002725 RCV000489986 RCV000588914 RCV002371754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000040.1:p.Ala305Glu
CA252356
NM_000049.4:c.914C>A