Canonical Allele Identifier: PA2825669159
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 802197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122062.3:p.Leu169Phe
CA3732447
NM_001128590.3:c.507A>T
CA363503793
NM_001128590.3:c.507A>C