Canonical Allele Identifier: PA2741845404
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2741979
ClinVar RCV Id: RCV003523598
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.His502Tyr
CA374105574
NM_001243743.2:c.1504C>T