Canonical Allele Identifier: PA2499238604
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 1121636
ClinVar RCV Id: RCV001451956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Val281Met
CA8289050
NM_001128085.1:c.841G>A