Canonical Allele Identifier: PA2827483261
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2635630
ClinVar RCV Id: RCV003427949 RCV003732578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336270.1:p.Thr389Ser
CA2491064
NM_001349341.3:c.1166C>G
CA2491065
NM_001349341.3:c.1165A>T