Canonical Allele Identifier: PA2828285926
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_001355072.1:p.Leu64Phe
CA3732447
NM_001368143.1:c.192A>T
CA363503793
NM_001368143.1:c.192A>C