Allele Registry

Canonical Allele Identifier: PA2825501667

Gene: CYP11A1 HGNC NCBI

ClinVar RCV:

RCV000019069

ClinVar Variation:

17517

HGVS (amino-acid)	Matching Registered Transcripts
NP_001093243.1:p.Arg195Trp	CA127237 NM_001099773.2:c.583C>T