Canonical Allele Identifier: PA658800208
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 526333
ClinVar RCV Id: RCV000630849 RCV001271599 RCV001821773 RCV002461940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ala797Val
CA8251738
NM_000135.4:c.2390C>T