Canonical Allele Identifier: PA1139710026
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 879121
ClinVar RCV Id: RCV001106326 RCV002240735 RCV003160633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Ile149Val
CA382619468
NM_003002.4:c.445A>G