Canonical Allele Identifier: PA2741834883
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 2514766
ClinVar RCV Id: RCV003248694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Asp275Glu
CA397687547
NM_001128085.1:c.825C>A
CA397687549
NM_001128085.1:c.825C>G