Canonical Allele Identifier: PA2827482480
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 217265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336269.1:p.Arg514Cys
CA351646
NM_001349340.3:c.1540C>T