Canonical Allele Identifier: PA159599
Gene: FANCG HGNC NCBI

Linked Data

ClinVar Variation Id: 134360
ClinVar RCV Id: RCV000121034 RCV000630846 RCV001271366 RCV001507747 RCV003153395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004620.1:p.Pro386Arg
CA159597
NM_004629.2:c.1157C>G