Canonical Allele Identifier: PA2573069373
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1319518
ClinVar RCV Id: RCV003237518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ser1383Ile
CA397484291
NM_001286167.3:c.4148G>T