Canonical Allele Identifier: PA645461471
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 362148
ClinVar RCV Id: RCV000332351 RCV000389302 RCV002504183
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Leu402Ser
CA10630459
NM_000497.4:c.1205T>C