Canonical Allele Identifier: PA2828286046
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 242688
ClinVar RCV Id: RCV001269964 RCV002250603 RCV002298552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355073.1:p.Met105Lys
CA358446
NM_001368144.1:c.314T>A