Canonical Allele Identifier: PA658808326
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 537389
ClinVar RCV Id: RCV000646226 RCV003411525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001444.2:p.Arg127His
CA362558693
NM_001453.3:c.380G>A