Allele Registry

Canonical Allele Identifier: PA118555

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000007327

RCV002228013

RCV002326667

RCV003472996

ClinVar Variation:

6918

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.His145Asn	CA016721 NM_003002.4:c.433C>A