Canonical Allele Identifier: PA355888
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 220016
ClinVar RCV Id: RCV000205662 RCV000564875 RCV001753610 RCV003407725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Arg535Cys
CA349793
NM_000136.3:c.1603C>T