Canonical Allele Identifier: PA2573203647
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1389317
ClinVar RCV Id: RCV001887129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Val109Met
CA8253064
NM_001351830.2:c.325G>A