Canonical Allele Identifier: PA2826558630
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 6895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Gly12Ser
CA016980
NM_001276506.2:c.34G>A