ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826080309
Gene: FOXP2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000175859
RCV000234933
RCV002336427
RCV003927612
ClinVar Variation:
195296
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001166237.1:p.Gln17Leu
CA241662
NM_001172766.3:c.50A>T