Allele Registry

Canonical Allele Identifier: PA2499229591

Gene: HSD11B2 HGNC NCBI

ClinVar RCV:

RCV001329093

ClinVar Variation:

1028126

HGVS (amino-acid)	Matching Registered Transcripts
NP_000187.3:p.Arg337Leu	CA396282986 NM_000196.4:c.1010G>T