Canonical Allele Identifier: PA645398135
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 239660
ClinVar RCV Id: RCV000227636 RCV000563763 RCV000409751 RCV000998351 RCV001158018 RCV001158017 RCV001158019 RCV004529398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004159.2:p.Ala660Gly
CA3173479
NM_004168.4:c.1979C>G