ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA658661890
Gene: FANCE
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000525524
RCV001821582
RCV002256387
ClinVar Variation:
471926
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_068741.1:p.Arg92Trp
CA3771370
NM_021922.3:c.274C>T