Canonical Allele Identifier: PA2828322022
Gene: FOXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 322414
ClinVar RCV Id: RCV000286412 RCV000432702 RCV001824734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356298.1:p.Arg69Cys
CA8459177
NM_001369369.1:c.205C>T