Canonical Allele Identifier: PA2830144856
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_476498.1:p.His233Arg
CA248447
NM_057157.2:c.698A>G