Canonical Allele Identifier: PA2580193570
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2417997
ClinVar RCV Id: RCV003118106
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Pro1393Ser
CA397483818
NM_001286167.3:c.4177C>T