Canonical Allele Identifier: PA1139686977
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 955187
ClinVar RCV Id: RCV001227782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ser1383Gly
CA397484294
NM_001286167.3:c.4147A>G