Canonical Allele Identifier: PA2825055416
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1329751
ClinVar RCV Id: RCV001800059 RCV002334701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Val154Gly
CA374338666
NM_000136.3:c.461T>G