Canonical Allele Identifier: PA107860
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 6896
ClinVar RCV Id: RCV000007303 RCV000007304 RCV000020519 RCV000162448 RCV000216073 RCV000763227 RCV002221470 RCV002228002 RCV003472995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Pro81Leu
CA016688
NM_003002.4:c.242C>T