Canonical Allele Identifier: PA299168
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 182479
ClinVar RCV Id: RCV000160480 RCV000459016 RCV001027088 RCV001274477
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Cys268Ser
CA299166
NM_000136.3:c.802T>A
CA374109250
NM_000136.3:c.803G>C