Canonical Allele Identifier: PA358572
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 224952
ClinVar RCV Id: RCV000216190 RCV000224380 RCV000282383 RCV000349064 RCV000374489 RCV000411625 RCV000573807 RCV001080211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004159.2:p.Gly6Asp
CA358571
NM_004168.4:c.17G>A