Canonical Allele Identifier: PA658660501
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 449254
ClinVar RCV Id: RCV000518928 RCV000687151 RCV001016395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ile91Val
CA5137785
NM_000136.3:c.271A>G