Canonical Allele Identifier: PA2825056252
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1338426
ClinVar RCV Id: RCV001817797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Lys545del
CA2573053198
NM_000136.3:c.1633_1635del