Canonical Allele Identifier: PA2826710803
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 862067

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Gly115Glu
CA8253057
NM_001286167.3:c.344G>A