Canonical Allele Identifier: PA2827482161
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 421700
ClinVar RCV Id: RCV000480408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336269.1:p.Leu355Pro
CA16618010
NM_001349340.3:c.1064T>C