Canonical Allele Identifier: PA915957819
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12175
ClinVar RCV Id: RCV000012957 RCV001851813 RCV003390673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000491.4:p.Arg427His
CA136895676
NM_000500.9:c.1280G>A