Canonical Allele Identifier: PA2741815752
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3046177
ClinVar RCV Id: RCV003951808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000491.4:p.Phe477Ser
CA136895689
NM_000500.9:c.1430T>C