Canonical Allele Identifier: PA2826924498
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 526376
ClinVar RCV Id: RCV000630898 RCV002255481 RCV001541811
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Ser20Cys
CA7168689
NM_001308133.2:c.59C>G