Canonical Allele Identifier: PA916009758
Gene: RIT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 181522
ClinVar Variation Id: 183407
ClinVar Variation Id: 370035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243750.1:p.Phe99Leu
CA297161
NM_001256821.2:c.297T>G
CA353877
NM_001256821.2:c.295T>C
CA16040628
NM_001256821.2:c.297T>A