Canonical Allele Identifier: PA2827481181
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2635630
ClinVar RCV Id: RCV003427949 RCV003732578
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336267.1:p.Thr390Ser
CA2491064
NM_001349338.3:c.1169C>G
CA2491065
NM_001349338.3:c.1168A>T