Canonical Allele Identifier: PA658800154
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_000126.2:p.Glu260Lys
CA8252812
NM_000135.4:c.778G>A