Canonical Allele Identifier: PA2580136738
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 2129207
ClinVar RCV Id: RCV003057961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Tyr231His
CA8289011
NM_001128085.1:c.691T>C