Canonical Allele Identifier: PA107860
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 6896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Pro81Leu
CA016688
NM_003002.4:c.242C>T