Canonical Allele Identifier: PA916014818
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134238
ClinVar RCV Id: RCV000120911 RCV000469548 RCV001115652 RCV001509536 RCV003905153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Gln286Arg
CA159229
NM_001286167.3:c.857A>G