Canonical Allele Identifier: PA645392802
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 265478
ClinVar RCV Id: RCV000255576 RCV000416497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001444.2:p.Leu86Phe
CA10588416
NM_001453.3:c.256C>T
CA2695205857
NM_001453.3:c.255_256delinsTT