Canonical Allele Identifier: PA2827481221
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_001336267.1:p.Pro413Ala
CA353493978
NM_001349338.3:c.1237C>G