Allele Registry

Canonical Allele Identifier: PA2573227484

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV001904371

ClinVar Variation:

1359268

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.Ser52Leu	CA382617105 NM_003002.4:c.155C>T