Canonical Allele Identifier: PA2826925137
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 526355
ClinVar RCV Id: RCV000630876 RCV002255480 RCV002469225 RCV002483772 RCV002528846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Pro694Ser
CA7169242
NM_001308133.2:c.2080C>T