Canonical Allele Identifier: PA253994
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_002993.1:p.Tyr93del
CA016628
NM_003002.4:c.278_280del
CA2615985385
NM_003002.4:c.276_278del