Canonical Allele Identifier: PA2825329282
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 498553
ClinVar RCV Id: RCV000593561 RCV001243169 RCV002483594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018122.1:p.Glu260Lys
CA8252812
NM_001018112.2:c.778G>A