Canonical Allele Identifier: PA2828286138
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12159
ClinVar RCV Id: RCV000012943 RCV000711371 RCV002288483 RCV003985261 RCV003924827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355073.1:p.Pro319Ser
CA341186
NM_001368144.1:c.955C>T