Canonical Allele Identifier: PA1139709928
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 840151
ClinVar RCV Id: RCV002239327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Leu76Pro
CA382617271
NM_003002.4:c.227T>C