Canonical Allele Identifier: PA916014953
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 526342
ClinVar RCV Id: RCV000630862 RCV001292817 RCV003478349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg756Pro
CA8251806
NM_001286167.3:c.2267G>C