Canonical Allele Identifier: PA645431405
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 241318
ClinVar RCV Id: RCV000227957 RCV001536588 RCV002256168 RCV004541448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Ile839Met
CA7169365
NM_020937.4:c.2517T>G