ClinGen Allele Registry
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Canonical Allele Identifier:
PA916015110
Gene: FANCA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
321335
ClinVar RCV Id:
RCV000287104
RCV000484383
RCV001094249
RCV003912330
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001273096.1:p.Arg1184Pro
CA8251098
NM_001286167.3:c.3551G>C