Canonical Allele Identifier: PA2825055557
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1341333
ClinVar RCV Id: RCV001836608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Leu215Phe
CA374109601
NM_000136.3:c.643C>T