Canonical Allele Identifier: PA916047148
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 802197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355073.1:p.Leu64Phe
CA3732447
NM_001368144.1:c.192A>T
CA363503793
NM_001368144.1:c.192A>C