Canonical Allele Identifier: PA2573191080
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1362014
ClinVar RCV Id: RCV001899965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ser1400Asn
CA397483625
NM_001286167.3:c.4199G>A