Canonical Allele Identifier: PA645461469
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 362149
ClinVar RCV Id: RCV000287487 RCV000344753 RCV001515368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Ala386Val
CA4905091
NM_000497.4:c.1157C>T