Canonical Allele Identifier: PA2580271638
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1739553
ClinVar RCV Id: RCV002331890 RCV003094637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Tyr144_His145del
CA2580083536
NM_003002.4:c.430_435del