Allele Registry

Canonical Allele Identifier: PA1139668213

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV001269684

ClinVar Variation:

988370

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Gln319Glu	CA363510515 NM_000500.9:c.955C>G