Canonical Allele Identifier: PA645400852
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 422748
ClinVar RCV Id: RCV000483808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Val21Ala
CA16618895
NM_000136.3:c.62T>C