Canonical Allele Identifier: PA2826926832
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 1684728
ClinVar RCV Id: RCV002247820
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295063.1:p.Glu524Gly
CA389592736
NM_001308134.2:c.1571A>G