Canonical Allele Identifier: PA2499244529
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1077797
ClinVar RCV Id: RCV002242999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Pro71Leu
CA382618953
NM_001276503.2:c.212C>T