Canonical Allele Identifier: PA2828285987
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12181
ClinVar RCV Id: RCV000012963
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355072.1:p.Gly241Ser
CA3732653
NM_001368143.1:c.721G>A