Canonical Allele Identifier: PA645441114
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 412512
ClinVar RCV Id: RCV001016345 RCV001252746 RCV002230664 RCV003235231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Ala90Glu
CA070965
NM_003002.4:c.269C>A