Canonical Allele Identifier: PA891845112
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 582335
ClinVar RCV Id: RCV000706384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Glu54Lys
CA374340196
NM_000136.3:c.160G>A