Canonical Allele Identifier: PA2573293079
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1422778
ClinVar RCV Id: RCV001926234 RCV002561328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116071.2:p.Ala412Thr
CA2491051
NM_032682.6:c.1234G>A