Canonical Allele Identifier: PA213399
Gene: HSD11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 31588
ClinVar RCV Id: RCV000024294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861420.1:p.Arg137Cys
CA213398
NM_181755.3:c.409C>T