Canonical Allele Identifier: PA159312
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134267
ClinVar RCV Id: RCV000120940 RCV000474415 RCV003444203 RCV003965014 RCV002293419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Leu1143Val
CA159310
NM_000135.4:c.3427C>G