Canonical Allele Identifier: PA2826710822
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1358367
ClinVar RCV Id: RCV001878607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Gln123Glu
CA397480964
NM_001286167.3:c.367C>G