Canonical Allele Identifier: PA2828286061
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 800926
ClinVar RCV Id: RCV000985129 RCV001269954 RCV003972997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355073.1:p.Met149Val
CA3732555
NM_001368144.1:c.445A>G