Canonical Allele Identifier: PA2573191081
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1651204
ClinVar RCV Id: RCV002155708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ser1402Pro
CA397483578
NM_001286167.3:c.4204T>C