Canonical Allele Identifier: PA159612
Gene: FANCG HGNC NCBI

Linked Data

ClinVar Variation Id: 134365
ClinVar RCV Id: RCV000121039 RCV000631014 RCV001166627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004620.1:p.Trp122Cys
CA159610
NM_004629.2:c.366G>C
CA373314543
NM_004629.2:c.366G>T