Canonical Allele Identifier: PA2825201170
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2582720
ClinVar RCV Id: RCV003333836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Ser281Asn
CA4905283
NM_000497.4:c.842G>A