Canonical Allele Identifier: PA2826558119
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 302481
ClinVar RCV Id: RCV000344579 RCV000571997 RCV000506525 RCV002229954 RCV002288968 RCV003475929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Ala18Val
CA071521
NM_001276503.2:c.53C>T