Canonical Allele Identifier: PA2573203652
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1464705
ClinVar RCV Id: RCV001963523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Gln123Lys
CA397480965
NM_001351830.2:c.367C>A