Canonical Allele Identifier: PA069892
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 222817
ClinVar RCV Id: RCV000208222 RCV000228322 RCV000283732 RCV000342145 RCV000396726 RCV000570331 RCV000411374 RCV002510820 RCV003474989
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004159.2:p.Thr277Met
CA069792
NM_004168.4:c.830C>T