Canonical Allele Identifier: PA2826558823
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1716502
ClinVar RCV Id: RCV002303543 RCV004005599
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Gly78Ser
CA382617277
NM_001276506.2:c.232G>A