ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827485639
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_001336273.1:p.Leu254Pro
CA16618010
NM_001349344.3:c.761T>C