Canonical Allele Identifier: PA2826714553
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2721366
ClinVar RCV Id: RCV003522385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Asn1398Lys
CA397483672
NM_001286167.3:c.4194C>G
CA397483675
NM_001286167.3:c.4194C>A