Canonical Allele Identifier: PA276953
Gene: FOXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 212710
ClinVar RCV Id: RCV000192344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003584.2:p.Ser49Leu
CA276951
NM_003593.3:c.146C>T