Allele Registry

Canonical Allele Identifier: PA645441011

Gene: SDHD HGNC NCBI

ClinVar Allele:

408270

ClinVar RCV:

RCV000485004

RCV000492287

RCV002526633

ClinVar Variation:

422629

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.Met1Leu