Canonical Allele Identifier: PA274085
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 188888
ClinVar RCV Id: RCV000169243 RCV000489399 RCV000780871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Gly27Arg
CA274084
NM_001128085.1:c.79G>A
CA397681165
NM_001128085.1:c.79G>C