Canonical Allele Identifier: PA2573227490
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1687625
ClinVar RCV Id: RCV002251308 RCV003774738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Pro81Arg
CA382617298
NM_003002.4:c.242C>G