Allele Registry

Canonical Allele Identifier: PA110534

Gene: CYP11A1 HGNC NCBI

ClinVar RCV:

RCV000019069

ClinVar Variation:

17517

HGVS (amino-acid)	Matching Registered Transcripts
NP_000772.2:p.Arg353Trp	CA127237 NM_000781.3:c.1057C>T