Canonical Allele Identifier: PA2826924942
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 1431687
ClinVar RCV Id: RCV001981844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.His485Gln
CA389592654
NM_001308133.2:c.1455T>A
CA389592655
NM_001308133.2:c.1455T>G