Allele Registry

Canonical Allele Identifier: PA2829412699

Gene: SDHD HGNC NCBI

ClinVar Variation Id: 2145185

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.Phe136Leu	CA228555696 NM_003002.4:c.408T>A CA382619248 NM_003002.4:c.406T>C CA382619258 NM_003002.4:c.408T>G