Canonical Allele Identifier: PA2825056204
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1775371
ClinVar RCV Id: RCV002405524

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ile522Met
CA374104712
NM_000136.3:c.1566C>G