Allele Registry

Canonical Allele Identifier: PA645441164

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000215839

ClinVar Variation:

231638

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.Tyr114Asn	CA10579347 NM_003002.4:c.340T>A