Canonical Allele Identifier: PA2741999447
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2635630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116071.2:p.Thr390Ser
CA2491064
NM_032682.6:c.1169C>G
CA2491065
NM_032682.6:c.1168A>T