Canonical Allele Identifier: PA916031200
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321375
ClinVar RCV Id: RCV000306986 RCV003477894
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Arg20Lys
CA8253263
NM_001351830.2:c.59G>A