ClinGen Allele Registry
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Canonical Allele Identifier:
PA192718
Gene: SDHD
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
183479
ClinVar RCV:
RCV000165195
RCV002228740
ClinVar Variation:
185719
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002993.1:p.His102Asn
CA016659
NM_003002.4:c.304C>A