ClinGen Allele Registry
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Canonical Allele Identifier:
PA645431293
Gene: FANCM
HGNC
NCBI
Linked Data
ClinVar Variation Id:
313196
ClinVar RCV Id:
RCV000353097
RCV001706480
RCV002258875
RCV004544556
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_065988.1:p.Glu309Ala
CA7168890
NM_020937.4:c.926A>C