Canonical Allele Identifier: PA091695
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 2605
ClinVar RCV Id: RCV000002723 RCV000420704 RCV000590467 RCV002444416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000040.1:p.Glu285Ala
CA325511
NM_000049.4:c.854A>C