Canonical Allele Identifier: PA212942
Gene: HSD11B2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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