ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA105520
Gene: HSD11B2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
12096
ClinVar RCV Id:
RCV000012877
RCV002508774
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000187.3:p.Arg208His
CA121882
NM_000196.4:c.623G>A