Canonical Allele Identifier: PA2825056209
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 651971
ClinVar RCV Id: RCV000807428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Gly524Ser
CA5137295
NM_000136.3:c.1570G>A