Canonical Allele Identifier: PA2825055562
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 3230392
ClinVar RCV Id: RCV004520543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Gln216Pro
CA374109594
NM_000136.3:c.647A>C