Canonical Allele Identifier: PA248403
Gene: FOXF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156707
ClinVar RCV Id: RCV000190285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001443.1:p.Ala300Gly
CA248402
NM_001452.2:c.899C>G