Canonical Allele Identifier: PA645400793
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 422569
ClinVar RCV Id: RCV000481288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Val6Leu
CA16618897
NM_000136.3:c.16G>C
CA374340519
NM_000136.3:c.16G>T