ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA107695
Gene: SDHB
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000216404
RCV000800486
RCV003335029
ClinVar Variation:
12785
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002991.2:p.Arg46Gly
CA015497
NM_003000.3:c.136C>G