Canonical Allele Identifier: PA915957341
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 550643
ClinVar RCV Id: RCV000665440 RCV002281122 RCV002477481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Arg341Ser
CA4905177
NM_001026213.1:c.1021C>A