ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645429122
Gene: FANCE
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000474134
RCV001821341
RCV002256300
ClinVar Variation:
414821
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_068741.1:p.Met437Thr
CA3771662
NM_021922.3:c.1310T>C