Allele Registry

Canonical Allele Identifier: PA111434

Gene: RIT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 181522

ClinVar RCV Id: RCV000054406 RCV000159101 RCV000207343 RCV001255602 RCV001375970 RCV001813414 RCV003398818 RCV003483526

ClinVar Variation Id: 183407

ClinVar RCV Id: RCV000207346 RCV000254958 RCV001813419 RCV001850287 RCV003317110 RCV003927532

ClinVar Variation Id: 370035

ClinVar RCV Id: RCV000408903 RCV000427451 RCV000856765 RCV003372696

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_008843.1:p.Phe82Leu	CA297161 NM_006912.6:c.246T>G CA353877 NM_006912.6:c.244T>C CA16040628 NM_006912.6:c.246T>A