ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA212942
Gene: HSD11B2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
27141
ClinVar RCV:
RCV000012884
ClinVar Variation:
12102
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000187.3:p.Tyr299del
CA212941
NM_000196.4:c.895_897del