Canonical Allele Identifier: PA106733
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_066124.1:p.Cys620Arg
CA008055
NM_020975.6:c.1858T>C
CA658761132
NM_020975.6:c.1857_1858delinsTC