Canonical Allele Identifier: PA2580271598
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1716502
ClinVar RCV Id: RCV002303543 RCV004005599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Gly78Ser
CA382617277
NM_003002.4:c.232G>A