ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826335930
Gene: FOXP1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2441549
ClinVar RCV Id:
RCV003144090
RCV003778881
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001231742.1:p.Ala464Thr
CA2490866
NM_001244813.1:c.1390G>A