Canonical Allele Identifier: PA915957333
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 552598
ClinVar RCV Id: RCV000667891 RCV003558494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Ala331Val
CA372394361
NM_001026213.1:c.992C>T