Canonical Allele Identifier: PA645438756
Gene: FANCG HGNC NCBI

Linked Data

ClinVar Variation Id: 435153
ClinVar RCV Id: RCV000500656 RCV000630991 RCV001294012 RCV001597147
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004620.1:p.Gln247Lys
CA5039969
NM_004629.2:c.739C>A