Canonical Allele Identifier: PA2829685980
Gene: SARDH HGNC NCBI

Linked Data

ClinVar Variation Id: 3157833
ClinVar RCV Id: RCV004450154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009032.2:p.Arg241His
CA5314691
NM_007101.3:c.722G>A