Canonical Allele Identifier: PA2826710838
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2981915
ClinVar RCV Id: RCV003840497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Thr126Ala
CA286608242
NM_001286167.3:c.376A>G