Canonical Allele Identifier: PA2825782064
Gene: SARDH HGNC NCBI

Linked Data

ClinVar Variation Id: 3157833
ClinVar RCV Id: RCV004450154
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128179.1:p.Arg241His
CA5314691
NM_001134707.2:c.722G>A