Canonical Allele Identifier: PA2826558441
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 412511
ClinVar RCV Id: RCV000562410 RCV001821298 RCV001584171 RCV002230663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Ala51Val
CA070974
NM_001276504.2:c.152C>T