Canonical Allele Identifier: PA2826558825
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 2452937
ClinVar RCV Id: RCV003177711
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Leu79Val
CA382617284
NM_001276506.2:c.235C>G