ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827484910
Gene: FOXP1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2062820
ClinVar RCV Id:
RCV002958031
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001336272.1:p.Leu313Val
CA76530288
NM_001349343.3:c.937C>G