Canonical Allele Identifier: PA915957788
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 804728
ClinVar RCV Id: RCV000991866 RCV001805959 RCV002488087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000491.4:p.Pro268Leu
CA3732545
NM_000500.9:c.803C>T