Canonical Allele Identifier: PA2828048885
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13922
ClinVar RCV Id: RCV000014947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Arg718Gly
CA009130
NM_001355216.1:c.2152A>G