Canonical Allele Identifier: PA2825056010
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 654075
ClinVar RCV Id: RCV000809967 RCV001010741 RCV001273984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Phe428del
CA915947017
NM_000136.3:c.1283_1285del