Canonical Allele Identifier: PA915989411
Gene: SARDH HGNC NCBI

Linked Data

ClinVar Variation Id: 730901
ClinVar RCV Id: RCV000905769
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009032.2:p.Arg280Gln
CA5314639
NM_007101.3:c.839G>A