Canonical Allele Identifier: PA645441113
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 412511
ClinVar RCV Id: RCV000562410 RCV001821298 RCV001584171 RCV002230663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Ala90Val
CA070974
NM_003002.4:c.269C>T