Canonical Allele Identifier: PA915971569
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 434880
ClinVar RCV Id: RCV000503594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122062.3:p.Trp23Cys
CA3732269
NM_001128590.3:c.69G>T
CA363498795
NM_001128590.3:c.69G>C