Canonical Allele Identifier: PA2826710778
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1398482
ClinVar RCV Id: RCV001893553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg104Lys
CA286608274
NM_001286167.3:c.311G>A