Canonical Allele Identifier: PA2825056250
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1052199
ClinVar RCV Id: RCV001360337

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ser543Pro
CA374104383
NM_000136.3:c.1627T>C