Canonical Allele Identifier: PA101014
Gene: FOXC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7260
ClinVar RCV Id: RCV000007682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005242.1:p.Ser125Leu
CA254126
NM_005251.3:c.374C>T