Canonical Allele Identifier: PA2741811975
Gene: HSD11B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2771416
ClinVar RCV Id: RCV003574260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000187.3:p.Phe185Leu
CA396279116
NM_000196.4:c.553T>C
CA396279128
NM_000196.4:c.555C>A
CA396279130
NM_000196.4:c.555C>G