ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825578487
Gene: FANCL
HGNC
NCBI
Linked Data
ClinVar Variation Id:
456243
ClinVar RCV Id:
RCV000552744
RCV001137464
RCV001821482
RCV003925582
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001108108.1:p.Arg68Pro
CA1670757
NM_001114636.1:c.203G>C