Canonical Allele Identifier: PA645389266
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 391588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116071.2:p.Phe502Leu
CA16604636
NM_032682.6:c.1506C>G
CA353492743
NM_032682.6:c.1506C>A
CA353492756
NM_032682.6:c.1504T>C