Canonical Allele Identifier: PA2826924865
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 945326
ClinVar RCV Id: RCV001215944

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Arg396Cys
CA7168979
NM_001308133.2:c.1186C>T