Canonical Allele Identifier: PA916015022
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134262
ClinVar RCV Id: RCV000120935 RCV000667206 RCV000872247
ClinVar Variation Id: 376974
ClinVar RCV Id: RCV000431238 RCV001080884 RCV001120358 RCV001821151 RCV003902464
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Asp953Glu
CA159296
NM_001286167.3:c.2859C>A
CA8251450
NM_001286167.3:c.2859C>G