Canonical Allele Identifier: PA2827628443
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134238
ClinVar RCV Id: RCV000120911 RCV000469548 RCV001115652 RCV001509536 RCV003905153
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Gln254Arg
CA159229
NM_001351830.2:c.761A>G