Allele Registry

Canonical Allele Identifier: PA2826558687

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV001994938

ClinVar Variation:

1462918

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263435.1:p.Ser32Leu	CA382616984 NM_001276506.2:c.95C>T