Canonical Allele Identifier: PA2825055968
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1431359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Met406Ile
CA5137419
NM_000136.3:c.1218G>C
CA374107445
NM_000136.3:c.1218G>T
CA374107446
NM_000136.3:c.1218G>A