Canonical Allele Identifier: PA915971582
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 585754
ClinVar RCV Id: RCV000711380 RCV003155292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122062.3:p.Thr94Ile
CA3732373
NM_001128590.3:c.281C>T