Canonical Allele Identifier: PA2826336751
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 55847
ClinVar RCV Id: RCV000049262 RCV000049263 RCV000175486 RCV000437146 RCV002311531 RCV003934994
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231743.1:p.Pro568Ser
CA201483
NM_001244814.1:c.1702C>T