Canonical Allele Identifier: PA645438789
Gene: FANCG HGNC NCBI

Linked Data

ClinVar Variation Id: 366730
ClinVar RCV Id: RCV000374615 RCV001095313
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004620.1:p.Ser603Phe
CA5039614
NM_004629.2:c.1808C>T