Canonical Allele Identifier: PA2580262014
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2269851
ClinVar RCV Id: RCV002804329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001444.2:p.Asp210Asn
CA362559234
NM_001453.3:c.628G>A