Allele Registry

Canonical Allele Identifier: PA111478

Gene: RIT1 HGNC NCBI

ClinVar Allele:

181505

ClinVar RCV:

RCV000207342

RCV000486847

RCV000707713

RCV001813421

RCV003965185

ClinVar Variation:

183411

HGVS (amino-acid)	Matching Registered Transcripts
NP_008843.1:p.Tyr89His	CA353873 NM_006912.6:c.265T>C