Canonical Allele Identifier: PA2580439387
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 2038723
ClinVar RCV Id: RCV002907696
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Glu1521Val
CA389608170
NM_020937.4:c.4562A>T