Canonical Allele Identifier: PA645431294
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 241314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Pro347Leu
CA7168910
NM_020937.4:c.1040C>T