Canonical Allele Identifier: PA916014972
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134258
ClinVar RCV Id: RCV000120931 RCV000668295 RCV000766439 RCV001447411 RCV003398726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Leu856Ser
CA159284
NM_001286167.3:c.2567T>C