Canonical Allele Identifier: PA2825056190
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 819542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.His520Gln
CA374104747
NM_000136.3:c.1560C>G
CA374104749
NM_000136.3:c.1560C>A