Canonical Allele Identifier: PA645431288
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 414846
ClinVar RCV Id: RCV000474146 RCV001292816 RCV002475907 RCV004541480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Ser175Pro
CA7168795
NM_020937.4:c.523T>C