Canonical Allele Identifier: PA2826329812
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 127541
ClinVar RCV Id: RCV000115352 RCV000315029 RCV000709093 RCV000571052 RCV001818267 RCV003492473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ala132Gly
CA287213
NM_001243743.2:c.395C>G