Canonical Allele Identifier: PA2825055031
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1362014
ClinVar RCV Id: RCV001899965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ala1399Thr
CA397483625
NM_000135.4:c.4195G>A