Canonical Allele Identifier: PA2826558837
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 239465
ClinVar RCV Id: RCV001854833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Ala83Val
CA070931
NM_001276506.2:c.248C>T