Canonical Allele Identifier: PA2825055016
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1361923
ClinVar RCV Id: RCV001899920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Gly1390Val
CA397483853
NM_000135.4:c.4169G>T