Canonical Allele Identifier: PA091700
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 371086
ClinVar RCV Id: RCV000411129 RCV003330657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000040.1:p.His244Arg
CA16041827
NM_000049.4:c.731A>G