Canonical Allele Identifier: PA2825028963
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 2156219
ClinVar RCV Id: RCV003090863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000040.1:p.Val154Ile
CA8288939
NM_000049.4:c.460G>A