Canonical Allele Identifier: PA2829412453
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 3075559
ClinVar RCV Id: RCV004017077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Gly58Val
CA382617158
NM_003002.4:c.173G>T