Canonical Allele Identifier: PA645431293
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 313196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Glu309Ala
CA7168890
NM_020937.4:c.926A>C