Canonical Allele Identifier: PA2826558509
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1734455
ClinVar RCV Id: RCV002349225

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Lys86Glu
CA382619040
NM_001276504.2:c.256A>G