Canonical Allele Identifier: PA2573280573
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 1431687
ClinVar RCV Id: RCV001981844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.His511Gln
CA389592654
NM_020937.4:c.1533T>A
CA389592655
NM_020937.4:c.1533T>G