Canonical Allele Identifier: PA2827484324
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 217265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336271.1:p.Arg414Cys
CA351646
NM_001349342.3:c.1240C>T