Canonical Allele Identifier: PA2826334389
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1422778
ClinVar RCV Id: RCV001926234 RCV002561328
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231739.1:p.Ala412Thr
CA2491051
NM_001244810.1:c.1234G>A