Canonical Allele Identifier: PA916015102
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 237050
ClinVar RCV Id: RCV000232454 RCV000765323
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Cys1159Ser
CA8251141
NM_001286167.3:c.3476G>C
CA397485896
NM_001286167.3:c.3475T>A