Canonical Allele Identifier: PA2826925366
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 313209
ClinVar RCV Id: RCV000271250 RCV000585067 RCV000763932 RCV001820928 RCV001843509 RCV001770252 RCV002255362 RCV004537778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Lys927Asn
CA7169420
NM_001308133.2:c.2781A>C
CA389599336
NM_001308133.2:c.2781A>T