Canonical Allele Identifier: PA916014792
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321366
ClinVar RCV Id: RCV000274943 RCV001094307 RCV001820959 RCV003922359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Val230Ile
CA8252857
NM_001286167.3:c.688G>A