Canonical Allele Identifier: PA645441150
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 412515
ClinVar RCV Id: RCV000565076 RCV001591105 RCV002230665 RCV003325203 RCV003476144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Val111Ile
CA071246
NM_003002.4:c.331G>A