Canonical Allele Identifier: PA2826558765
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 859430
ClinVar RCV Id: RCV002240519
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Gly58Ser
CA382617155
NM_001276506.2:c.172G>A