Canonical Allele Identifier: PA2826558231
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 480806
ClinVar RCV Id: RCV000561906 RCV000660262 RCV002232089 RCV003420005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Ala58Ser
CA382618730
NM_001276503.2:c.172G>T