Canonical Allele Identifier: PA2829939072
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 423618
ClinVar RCV Id: RCV000479274 RCV000541134 RCV002356788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Pro20dup
CA16618957
NM_020630.6:c.59_61dup