Canonical Allele Identifier: PA2826558590
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 422629
ClinVar RCV Id: RCV000485004 RCV000492287 RCV002526633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Met1Leu