Canonical Allele Identifier: PA2580439394
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 2079135
ClinVar RCV Id: RCV002982732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Asn1531Asp
CA389608230
NM_020937.4:c.4591A>G