Canonical Allele Identifier: PA915975145
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 655492
ClinVar RCV Id: RCV000811684 RCV004028737
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Gly78Arg
CA382617278
NM_003002.4:c.232G>C