Canonical Allele Identifier: PA2828286033
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 596309
ClinVar RCV Id: RCV000732097 RCV000826138 RCV003975283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355072.1:p.Pro348Ser
CA3732730
NM_001368143.1:c.1042C>T