Canonical Allele Identifier: PA658666420
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 465235

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Gly12Asp
CA071285
NM_003002.4:c.35G>A