ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826926351
Gene: FANCM
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
464041
ClinVar RCV:
RCV000554625
RCV000763926
RCV000989207
RCV001770408
RCV001821483
RCV003338648
ClinVar Variation:
456276
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001295063.1:p.Arg18Gln
CA7168688
NM_001308134.2:c.53G>A