Canonical Allele Identifier: PA915980666
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 640532
ClinVar RCV Id: RCV000793577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001444.2:p.Tyr115Cys
CA362558608
NM_001453.3:c.344A>G