Canonical Allele Identifier: PA2741815726
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3056254
ClinVar RCV Id: RCV003978961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000491.4:p.Val398Ile
CA3732666
NM_000500.9:c.1192G>A