Canonical Allele Identifier: PA2825055332
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 946069
ClinVar RCV Id: RCV001216856 RCV002451484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ile114Leu
CA374339171
NM_000136.3:c.340A>T
CA374339174
NM_000136.3:c.340A>C