Allele Registry

Canonical Allele Identifier: PA2826925137

Gene: FANCM HGNC NCBI

ClinVar Allele:

528133

ClinVar RCV:

RCV000630876

RCV002255480

RCV002469225

RCV002483772

RCV002528846

ClinVar Variation:

526355

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