Canonical Allele Identifier: PA1139694478
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 853866
ClinVar RCV Id: RCV001058771

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Asp144Glu
CA374338744
NM_001243744.2:c.432T>G
CA374338745
NM_001243744.2:c.432T>A