Allele Registry

Canonical Allele Identifier: PA118554

Gene: SDHD HGNC NCBI

ClinVar Allele:

21950

ClinVar RCV:

RCV002228010

RCV004018582

ClinVar Variation:

6911

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.Met1Val