Canonical Allele Identifier: PA2580271584
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1778958
ClinVar RCV Id: RCV002399175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Gly58Arg
CA382617154
NM_003002.4:c.172G>C