Canonical Allele Identifier: PA2826558589
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 6906
ClinVar RCV Id: RCV000007315 RCV000020522 RCV000492533 RCV002228007
ClinVar Variation Id: 579968
ClinVar RCV Id: RCV002232947 RCV002369946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Met1Ile