Canonical Allele Identifier: PA2826925881
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 2079135
ClinVar RCV Id: RCV002982732
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Asn1505Asp
CA389608230
NM_001308133.2:c.4513A>G