Canonical Allele Identifier: PA2826926900
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 2142037
ClinVar RCV Id: RCV003074103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295063.1:p.Asn604Asp
CA7169164
NM_001308134.2:c.1810A>G