Canonical Allele Identifier: PA2826558454
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 6905
ClinVar RCV Id: RCV000007314 RCV002433446
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Tyr54del
CA016628
NM_001276504.2:c.161_163del
CA2615985385
NM_001276504.2:c.159_161del