Canonical Allele Identifier: PA916015060
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408205
ClinVar RCV Id: RCV000472481 RCV001276510 RCV001821268 RCV001509531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg1053Cys
CA8251319
NM_001286167.3:c.3157C>T