Canonical Allele Identifier: PA2827485119
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 217265
ClinVar RCV Id: RCV000207490 RCV001267938 RCV003417726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336272.1:p.Arg413Cys
CA351646
NM_001349343.3:c.1237C>T