Canonical Allele Identifier: PA159392
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 134297
ClinVar RCV Id: RCV000120970 RCV000590373 RCV000988196 RCV001169818 RCV001082312 RCV001357248 RCV000574575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Gln465Arg
CA159390
NM_000136.3:c.1394A>G