Canonical Allele Identifier: PA2826335052
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1422778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231741.1:p.Ala336Thr
CA2491051
NM_001244812.1:c.1006G>A