Canonical Allele Identifier: PA916015131
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408201
ClinVar RCV Id: RCV000463994 RCV002496760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ala1233Val
CA8251016
NM_001286167.3:c.3698C>T