Canonical Allele Identifier: PA2828439966
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 55847
ClinVar RCV Id: RCV000049262 RCV000049263 RCV000175486 RCV000437146 RCV002311531 RCV003934994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357477.1:p.Pro467Ser
CA201483
NM_001370548.1:c.1399C>T