Canonical Allele Identifier: PA2828285967
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1422248
ClinVar RCV Id: RCV001919442 RCV003978421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355072.1:p.Arg207Trp
CA3732615
NM_001368143.1:c.619C>T