Allele Registry

Canonical Allele Identifier: PA2826574582

Gene: CYP26B1 HGNC NCBI

ClinVar RCV:

RCV001538165

ClinVar Variation:

1180923

HGVS (amino-acid)	Matching Registered Transcripts
NP_001264671.1:p.Leu189Ser	CA1707951 NM_001277742.2:c.566T>C