Canonical Allele Identifier: PA2826710391
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408164
ClinVar RCV Id: RCV000470449 RCV003237862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Asn8Ser
CA8253274
NM_001286167.3:c.23A>G