Allele Registry

Canonical Allele Identifier: PA2499285633

Gene: CYP26B1 HGNC NCBI

ClinVar RCV:

RCV001538165

ClinVar Variation:

1180923

HGVS (amino-acid)	Matching Registered Transcripts
NP_063938.1:p.Leu264Ser	CA1707951 NM_019885.4:c.791T>C