Canonical Allele Identifier: PA2580136685
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 1928676
ClinVar RCV Id: RCV002635094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Cys152Ser
CA397682717
NM_001128085.1:c.454T>A
CA397682720
NM_001128085.1:c.455G>C