Allele Registry

Canonical Allele Identifier: PA212942

Gene: HSD11B2 HGNC NCBI

ClinVar RCV:

RCV000012884

ClinVar Variation:

12102

HGVS (amino-acid)	Matching Registered Transcripts
NP_000187.3:p.Tyr299del	CA212941 NM_000196.4:c.895_897del