Canonical Allele Identifier: PA273960
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 188788
ClinVar RCV Id: RCV000169117 RCV001293576 RCV002222420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Gly274Arg
CA273959
NM_001128085.1:c.820G>A
CA397687523
NM_001128085.1:c.820G>C