Canonical Allele Identifier: PA2826558768
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1778958
ClinVar RCV Id: RCV002399175
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Gly58Arg
CA382617154
NM_001276506.2:c.172G>C