Canonical Allele Identifier: PA2828286079
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1341485
ClinVar RCV Id: RCV003318405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355073.1:p.Arg205His
CA3732614
NM_001368144.1:c.614G>A