Canonical Allele Identifier: PA915957337
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 35980
ClinVar RCV Id: RCV000029636 RCV002513246
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Ala339Val
CA213650
NM_001026213.1:c.1016C>T