ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828322022
Gene: FOXN1
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000286412
RCV000432702
RCV001824734
ClinVar Variation:
322414
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001356298.1:p.Arg69Cys
CA8459177
NM_001369369.1:c.205C>T