Canonical Allele Identifier: PA2828439838
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1305023
ClinVar RCV Id: RCV001765198
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357477.1:p.Pro313Ala
CA353493978
NM_001370548.1:c.937C>G