Canonical Allele Identifier: PA645383491
Gene: ARAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001645.1:p.Ser214Cys
CA16602595
NM_001654.5:c.641C>G
CA645603172
NM_001654.5:c.641_642delinsGT