Canonical Allele Identifier: PA2826924795
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 241314
ClinVar RCV Id: RCV000233464 RCV001570689 RCV002255337 RCV001820757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Pro321Leu
CA7168910
NM_001308133.2:c.962C>T