Canonical Allele Identifier: PA2826574615
Gene: CYP26B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 445321
ClinVar RCV Id: RCV000514998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264671.1:p.Ala345Gly
CA1707795
NM_001277742.2:c.1034C>G