Canonical Allele Identifier: PA645381492
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 225335
ClinVar RCV Id: RCV000490344 RCV001357310 RCV003155127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000491.4:p.Ala392Thr
CA3732662
NM_000500.9:c.1174G>A