ClinGen Allele Registry
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Canonical Allele Identifier:
PA645431349
Gene: FANCM
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
320553
ClinVar RCV:
RCV000269296
RCV000763930
RCV001030474
RCV001292875
RCV001590938
RCV004537777
ClinVar Variation:
313200
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_065988.1:p.Arg581Cys
CA7169137
NM_020937.4:c.1741C>T