Canonical Allele Identifier: PA2825056185
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1399718
ClinVar RCV Id: RCV001893869 RCV002397871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Glu517Asp
CA374104796
NM_000136.3:c.1551G>T
CA374104797
NM_000136.3:c.1551G>C