Canonical Allele Identifier: PA2825056201
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1034879
ClinVar RCV Id: RCV001337668 RCV003294323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Glu521Asp
CA374104728
NM_000136.3:c.1563G>T
CA374104729
NM_000136.3:c.1563G>C