Canonical Allele Identifier: PA916015211
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321327
ClinVar RCV Id: RCV000299065 RCV001242774 RCV001731595 RCV004021684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.His1355Leu
CA8250797
NM_001286167.3:c.4064A>T