Canonical Allele Identifier: PA916014910
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 456087
ClinVar RCV Id: RCV000555138 RCV002293448 RCV002476088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ala624Gly
CA8251997
NM_001286167.3:c.1871C>G