ClinGen Allele Registry
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Canonical Allele Identifier:
PA645431497
Gene: FANCM
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000231642
RCV000253417
RCV000658692
RCV001331161
RCV002257595
ClinVar Variation:
241324
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_065988.1:p.Ile1742Val
CA7169934
NM_020937.4:c.5224A>G