Canonical Allele Identifier: PA358447
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 242688
ClinVar RCV Id: RCV001269964 RCV002250603 RCV002298552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000491.4:p.Met240Lys
CA358446
NM_000500.9:c.719T>A