Canonical Allele Identifier: PA170779
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 156153
ClinVar RCV Id: RCV000144171 RCV000484125 RCV001290090 RCV002415627 RCV002515941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Glu69Lys
CA016681
NM_003002.4:c.205G>A