Canonical Allele Identifier: PA2828047533
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13915
ClinVar RCV Id: RCV000014935 RCV000182580 RCV000232285 RCV000568259 RCV000736276 RCV003324711 RCV000826204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Cys366Arg
CA008055
NM_001355216.1:c.1096T>C
CA658761132
NM_001355216.1:c.1095_1096delinsTC