ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826335052
Gene: FOXP1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1422778
ClinVar RCV Id:
RCV001926234
RCV002561328
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001231741.1:p.Ala336Thr
CA2491051
NM_001244812.1:c.1006G>A