Canonical Allele Identifier: PA2826926003
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 526466
ClinVar RCV Id: RCV000631000 RCV001030553 RCV001797116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Glu1650Lys
CA7169893
NM_001308133.2:c.4948G>A