Canonical Allele Identifier: PA2826714552
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2116378
ClinVar RCV Id: RCV003024691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Asp1397Glu
CA397483695
NM_001286167.3:c.4191T>G
CA397483698
NM_001286167.3:c.4191T>A