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