Canonical Allele Identifier: PA2828286138
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355073.1:p.Pro319Ser
CA341186
NM_001368144.1:c.955C>T