Canonical Allele Identifier: PA277885
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 218581
ClinVar RCV Id: RCV000202919 RCV000575031 RCV001105197 RCV003103746
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Ile40Leu
CA277884
NM_003002.4:c.118A>C