Canonical Allele Identifier: PA915957330
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1173
ClinVar RCV Id: RCV000001232 RCV001066246 RCV002504733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Thr318Met
CA339876
NM_001026213.1:c.953C>T