Canonical Allele Identifier: PA2825669231
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3056254
ClinVar RCV Id: RCV003978961
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122062.3:p.Val368Ile
CA3732666
NM_001128590.3:c.1102G>A