Canonical Allele Identifier: PA2829215464
Gene: RASSF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2622660
ClinVar RCV Id: RCV004360395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001381029.1:p.Arg36Gln
CA234205153
NM_001394100.1:c.107G>A