Canonical Allele Identifier: PA106722
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24901
ClinVar RCV Id: RCV000163667 RCV000429944 RCV000423173 RCV000434317 RCV000440162 RCV000475953 RCV000424049 RCV001565486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Cys618Tyr
CA008005
NM_020975.6:c.1853G>A