Canonical Allele Identifier: PA212942
Gene: HSD11B2 HGNC NCBI

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Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_000187.3:p.Tyr299del
NM_000196.4:c.895_897del

NM_000196.4:c.[895_897del;900C>A]

NM_000196.4:c.[895_897del;900C=]

NM_000196.4:c.[895_897del;900C>T]