Canonical Allele Identifier: PA658827325
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 556405
ClinVar RCV Id: RCV000672406 RCV002531315 RCV004544930 RCV004526748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Arg454His
CA4905010
NM_000497.4:c.1361G>A