Canonical Allele Identifier: PA353882
Gene: RIT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 183410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008843.1:p.Ala84Val
CA353881
NM_006912.6:c.251C>T