Canonical Allele Identifier: PA2826558162
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 135196
ClinVar RCV Id: RCV000122008 RCV002228410 RCV000569765 RCV003997358 RCV001545828 RCV003230259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Phe34Cys
CA016754
NM_001276503.2:c.101T>G