Canonical Allele Identifier: PA2826926857
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 456254
ClinVar RCV Id: RCV000536634 RCV001293939 RCV001584242 RCV001800738 RCV002255431 RCV003492091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295063.1:p.Asp556Gly
CA7169123
NM_001308134.2:c.1667A>G