Canonical Allele Identifier: PA645402713
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 234582
ClinVar RCV Id: RCV000220014 RCV000456548 RCV000709081 RCV000988198 RCV001011135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ala455Ser
CA5137339
NM_000136.3:c.1363G>T