Canonical Allele Identifier: PA119640
Gene: FOXC1 HGNC NCBI
ClinVar RCV:
RCV000008978
ClinVar Variation:
8458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001444.2:p.Ser82Thr
CA119639
NM_001453.3:c.245G>C