Canonical Allele Identifier: PA658800341
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 526383
ClinVar RCV Id: RCV000630907 RCV001017222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Arg361Gln
CA5137460
NM_000136.3:c.1082G>A