Canonical Allele Identifier: PA2825202130
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 800573
ClinVar RCV Id: RCV000984551
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000491.4:p.Pro46Arg
CA363499178
NM_000500.9:c.137C>G