Canonical Allele Identifier: PA2573186895
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1431359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Met406Ile
CA5137419
NM_001243744.2:c.1218G>C
CA374107445
NM_001243744.2:c.1218G>T
CA374107446
NM_001243744.2:c.1218G>A