Canonical Allele Identifier: PA2826710472
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321375
ClinVar RCV Id: RCV000306986 RCV003477894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg20Lys
CA8253263
NM_001286167.3:c.59G>A