Canonical Allele Identifier: PA916014776
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134289
ClinVar RCV Id: RCV000120962 RCV000461615 RCV000664733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ser208Leu
CA159367
NM_001286167.3:c.623C>T