Canonical Allele Identifier: PA1139668115
Gene: CYP11B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 853826
ClinVar RCV Id: RCV001058716 RCV002497435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000489.3:p.Thr318Met
CA4906032
NM_000498.3:c.953C>T