Canonical Allele Identifier: PA1139684064
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 93160
ClinVar RCV Id: RCV000079017 RCV000711375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122062.3:p.Leu10del
CA214451
NM_001128590.3:c.29_31del