Canonical Allele Identifier: PA2826558474
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 3070901
ClinVar RCV Id: RCV004014403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Thr61Ser
CA382617403
NM_001276504.2:c.181A>T
CA382617405
NM_001276504.2:c.182C>G