Canonical Allele Identifier: PA916014835
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 456147
ClinVar RCV Id: RCV000527193 RCV000673548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Leu324Arg
CA397469937
NM_001286167.3:c.971T>G