Canonical Allele Identifier: PA335661
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 216281
ClinVar RCV Id: RCV000195408 RCV001017074 RCV001292900 RCV001546836 RCV002282033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Met350Val
CA335659
NM_000136.3:c.1048A>G