Canonical Allele Identifier: PA2741815627
Gene: CYP11B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2581484
ClinVar RCV Id: RCV003331889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000489.3:p.Ser315Arg
CA372388382
NM_000498.3:c.945C>G
CA372388383
NM_000498.3:c.945C>A
CA372388392
NM_000498.3:c.943A>C