Canonical Allele Identifier: PA2580271649
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 2032648
ClinVar RCV Id: RCV002881330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Lys158_Leu159delinsAsnPhe
CA2580083599
NM_003002.4:c.474_475delinsTT