Canonical Allele Identifier: PA2825201156
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 908222
ClinVar RCV Id: RCV001158582 RCV001158583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Asp268Asn
CA4905294
NM_000497.4:c.802G>A