Canonical Allele Identifier: PA2829412574
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1376583
ClinVar RCV Id: RCV001886002 RCV003355601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Leu101Phe
CA382617408
NM_003002.4:c.301C>T