ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825669245
Gene: CYP21A2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
12175
ClinVar RCV Id:
RCV000012957
RCV001851813
RCV003390673
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001122062.3:p.Arg397His
CA136895676
NM_001128590.3:c.1190G>A