Canonical Allele Identifier: PA2741978907
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 2825621
ClinVar RCV Id: RCV003637284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Asp1532Asn
CA389608237
NM_020937.4:c.4594G>A