ClinGen Allele Registry
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Canonical Allele Identifier:
PA658661714
Gene: FANCM
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000526327
RCV001591192
RCV002257786
RCV003316678
RCV004541643
ClinVar Variation:
456253
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_065988.1:p.Arg756His
CA7169305
NM_020937.4:c.2267G>A