Canonical Allele Identifier: PA2580183948
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_001263433.1:p.Leu92Phe
CA382619165
NM_001276504.2:c.274C>T