Canonical Allele Identifier: PA2826924848
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 526357
ClinVar RCV Id: RCV000630878 RCV002289919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Asp382His
CA7168972
NM_001308133.2:c.1144G>C