Canonical Allele Identifier: PA2573186764
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1387668
ClinVar RCV Id: RCV001884172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Arg271Ser
CA374109231
NM_001243744.2:c.813G>T
CA374109232
NM_001243744.2:c.813G>C