Canonical Allele Identifier: PA1139680403
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 873016
ClinVar RCV Id: RCV001260954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Ser120Phe
CA397682333
NM_001128085.1:c.359C>T