Canonical Allele Identifier: PA2829412684
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 2452938
ClinVar RCV Id: RCV003177712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Leu131Phe
CA382619165
NM_003002.4:c.391C>T