Canonical Allele Identifier: PA2825056053
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2560854
ClinVar RCV Id: RCV003288292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Val446Met
CA374106284
NM_000136.3:c.1336G>A