Canonical Allele Identifier: PA658807158
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 533788
ClinVar RCV Id: RCV002233496 RCV002440284 RCV004003915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Ala97Val
CA071022
NM_003002.4:c.290C>T