Canonical Allele Identifier: PA2580176567
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2040713
ClinVar RCV Id: RCV002890746
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Lys47Asn
CA374340242
NM_001243744.2:c.141G>T
CA374340243
NM_001243744.2:c.141G>C