Canonical Allele Identifier: PA2573191684
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1359777
ClinVar RCV Id: RCV001904546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Thr96Ile
CA382619243
NM_001276504.2:c.287C>T