ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827481128
Gene: FOXP1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
421700
ClinVar RCV Id:
RCV000480408
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001336267.1:p.Leu355Pro
CA16618010
NM_001349338.3:c.1064T>C