Canonical Allele Identifier: PA2826924952
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 848526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Gln496His
CA7169084
NM_001308133.2:c.1488G>T
CA389592723
NM_001308133.2:c.1488G>C