Canonical Allele Identifier: PA2825202184
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 802197
ClinVar RCV Id: RCV000987668 RCV000991864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000491.4:p.Leu199Phe
CA3732447
NM_000500.9:c.597A>T
CA363503793
NM_000500.9:c.597A>C