Canonical Allele Identifier: PA091691
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 2606
ClinVar RCV Id: RCV000002724 RCV003387712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000040.1:p.Cys152Arg
CA252354
NM_000049.4:c.454T>C