Canonical Allele Identifier: PA2741999443
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2989815
ClinVar RCV Id: RCV003842446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116071.2:p.Arg361Cys
CA2491106
NM_032682.6:c.1081C>T