ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA107743
Gene: SDHB
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000013628
RCV001021521
RCV001857343
ClinVar Variation:
12787
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002991.2:p.His132Pro
CA015817
NM_003000.3:c.395A>C