Canonical Allele Identifier: PA2741980671
Gene: NR2F2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2662617
ClinVar RCV Id: RCV003441282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066285.1:p.Ser101Gly
CA393930053
NM_021005.4:c.301A>G