Canonical Allele Identifier: PA913194510
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 596309
ClinVar RCV Id: RCV000732097 RCV000826138 RCV003975283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000491.4:p.Pro483Ser
CA3732730
NM_000500.9:c.1447C>T