Canonical Allele Identifier: PA1139737420
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 848526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Gln522His
CA7169084
NM_020937.4:c.1566G>T
CA389592723
NM_020937.4:c.1566G>C