Canonical Allele Identifier: PA248448
Gene: CYP26A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 208185
ClinVar RCV Id: RCV000190381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000774.2:p.His302Arg
CA248447
NM_000783.4:c.905A>G