Canonical Allele Identifier: PA891848324
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 578342
ClinVar RCV Id: RCV000764955 RCV002233358 RCV000986023 RCV003165869 RCV003999713
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Tyr141His
CA382619325
NM_003002.4:c.421T>C