Canonical Allele Identifier: PA2580262013
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2083699
ClinVar RCV Id: RCV003009186 RCV003358043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001444.2:p.Gln208Arg
CA3614796
NM_001453.3:c.623A>G