Canonical Allele Identifier: PA645441109
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 239465
ClinVar RCV Id: RCV001854833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Ala83Val
CA070931
NM_003002.4:c.248C>T