Canonical Allele Identifier: PA658803914
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 522484
ClinVar RCV Id: RCV000625626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Glu343Lys
CA372394111
NM_000497.4:c.1027G>A