Canonical Allele Identifier: PA2826335268
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 55847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231741.1:p.Pro492Ser
CA201483
NM_001244812.1:c.1474C>T