ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828322219
Gene: FOXN1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000434343
ClinVar Variation:
392379
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001356298.1:p.His321Arg
CA16607552
NM_001369369.1:c.962A>G