Canonical Allele Identifier: PA645441092
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 239463

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Arg70Lys
CA070846
NM_003002.4:c.209G>A