Canonical Allele Identifier: PA2826002902
Gene: RASSF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2622660
ClinVar RCV Id: RCV004360395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158219.1:p.Arg36Gln
CA234205153
NM_001164747.2:c.107G>A