Canonical Allele Identifier: PA2573203659
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1692223
ClinVar RCV Id: RCV002257107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Thr126Ser
CA397480946
NM_001351830.2:c.376A>T