Canonical Allele Identifier: PA111478
Gene: RIT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 183411
ClinVar RCV Id: RCV000207342 RCV000486847 RCV000707713 RCV001813421 RCV003965185
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Amino-acid Alleles

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