Canonical Allele Identifier: PA2828286108
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 800597
ClinVar RCV Id: RCV000984575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355073.1:p.Gln255His
CA363511322
NM_001368144.1:c.765A>T
CA363511323
NM_001368144.1:c.765A>C