Canonical Allele Identifier: PA1139694287
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 837120
ClinVar RCV Id: RCV001038389 RCV002427489 RCV003238276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Leu8Pro
CA5137849
NM_001243744.2:c.23T>C