Canonical Allele Identifier: PA2826558792
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 640150
ClinVar RCV Id: RCV002536951
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Thr67Asn
CA382617214
NM_001276506.2:c.200C>A