Canonical Allele Identifier: PA2827485645
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2989815
ClinVar RCV Id: RCV003842446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336273.1:p.Arg260Cys
CA2491106
NM_001349344.3:c.778C>T