Canonical Allele Identifier: PA915957790
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_000491.4:p.Met284Val
CA3732555
NM_000500.9:c.850A>G