Canonical Allele Identifier: PA2826558422
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 135198
ClinVar RCV Id: RCV000122010 RCV000568887 RCV002515893
ClinVar Variation Id: 412501
ClinVar RCV Id: RCV000562051 RCV000508222 RCV001328335 RCV003476141 RCV002230195 RCV003153649 RCV004002008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Leu46Phe
CA016696
NM_001276504.2:c.138G>T
CA070935
NM_001276504.2:c.138G>C