Canonical Allele Identifier: PA2826558106
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 2929526
ClinVar RCV Id: RCV003784692

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Gly15Glu
CA382616741
NM_001276503.2:c.44G>A