Canonical Allele Identifier: PA2825200929
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2051667
ClinVar RCV Id: RCV002927426 RCV002927427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Val129Leu
CA4905537
NM_000497.4:c.385G>C
CA4905538
NM_000497.4:c.385G>T