Canonical Allele Identifier: PA2826329843
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 127543
ClinVar RCV Id: RCV000115355 RCV000204580 RCV001024091 RCV001167421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ala181Val
CA287220
NM_001243743.2:c.542C>T