Canonical Allele Identifier: PA2826926830
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 848526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295063.1:p.Gln522His
CA7169084
NM_001308134.2:c.1566G>T
CA389592723
NM_001308134.2:c.1566G>C