Canonical Allele Identifier: PA2826338220
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 873452
ClinVar RCV Id: RCV001095670
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231745.1:p.Tyr470Phe
CA353493237
NM_001244816.1:c.1409A>T