Canonical Allele Identifier: PA658655078
Gene: CYP26B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 445321
ClinVar RCV Id: RCV000514998
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063938.1:p.Ala420Gly
CA1707795
NM_019885.4:c.1259C>G