Canonical Allele Identifier: PA2825782074
Gene: SARDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2508744
ClinVar RCV Id: RCV004287866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128179.1:p.Arg300Cys
CA5314621
NM_001134707.2:c.898C>T