Canonical Allele Identifier: PA2825055396
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 853866
ClinVar RCV Id: RCV001058771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Asp144Glu
CA374338744
NM_000136.3:c.432T>G
CA374338745
NM_000136.3:c.432T>A