Canonical Allele Identifier: PA2829412573
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 3070901
ClinVar RCV Id: RCV004014403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Thr100Ser
CA382617403
NM_003002.4:c.298A>T
CA382617405
NM_003002.4:c.299C>G