Canonical Allele Identifier: PA2825055351
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2562115
ClinVar RCV Id: RCV003310175
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ile121Thr
CA5137753
NM_000136.3:c.362T>C