Canonical Allele Identifier: PA2825056063
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1017642
ClinVar RCV Id: RCV001316820 RCV002384400 RCV002486246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.His452Arg
CA374106246
NM_000136.3:c.1355A>G