Canonical Allele Identifier: PA2826926506
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 414850
ClinVar RCV Id: RCV000463663 RCV001555524 RCV002256303 RCV004541481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295063.1:p.His164Pro
CA7168773
NM_001308134.2:c.491A>C