Canonical Allele Identifier: PA274161
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 188940
ClinVar RCV Id: RCV000169314 RCV001093138 RCV002265654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Pro181Thr
CA274160
NM_001128085.1:c.541C>A