Canonical Allele Identifier: PA916006977
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 234480
ClinVar RCV Id: RCV000221352 RCV001026491 RCV000630840 RCV001274480 RCV001797687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Leu250Ile
CA5137638
NM_001243744.2:c.748C>A