Canonical Allele Identifier: PA2499262950
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1060148
ClinVar RCV Id: RCV002242642 RCV002329384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Cys140Tyr
CA382619315
NM_003002.4:c.419G>A