Canonical Allele Identifier: PA213651
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 35980
ClinVar RCV Id: RCV000029636 RCV002513246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Ala339Val
CA213650
NM_000497.4:c.1016C>T