Canonical Allele Identifier: PA111450
Gene: RIT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 183401
ClinVar RCV Id: RCV000207341 RCV000255076 RCV000475746 RCV003235080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008843.1:p.Ser35Thr
CA353872
NM_006912.6:c.104G>C