ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827483211
Gene: FOXP1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000480408
ClinVar Variation:
421700
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001336270.1:p.Leu354Pro
CA16618010
NM_001349341.3:c.1061T>C