Canonical Allele Identifier: PA2826926969
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 456258
ClinVar RCV Id: RCV000529036 RCV003231525 RCV004537898
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295063.1:p.Arg666Gly
CA7169200
NM_001308134.2:c.1996A>G