Canonical Allele Identifier: PA2741826185
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2582720
ClinVar RCV Id: RCV003333836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Ser281Asn
CA4905283
NM_001026213.1:c.842G>A