Canonical Allele Identifier: PA916031227
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 552870
ClinVar RCV Id: RCV000668215 RCV001246549
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Gly115Arg
CA8253058
NM_001351830.2:c.343G>A
CA397481011
NM_001351830.2:c.343G>C