Canonical Allele Identifier: PA351647
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 217265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116071.2:p.Arg514Cys
CA351646
NM_032682.6:c.1540C>T