Canonical Allele Identifier: PA2828286111
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3056254
ClinVar RCV Id: RCV003978961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355073.1:p.Val263Ile
CA3732666
NM_001368144.1:c.787G>A