Canonical Allele Identifier: PA2825669229
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 225335
ClinVar RCV Id: RCV000490344 RCV001357310 RCV003155127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122062.3:p.Ala362Thr
CA3732662
NM_001128590.3:c.1084G>A