Canonical Allele Identifier: PA2829939368
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 3227540
ClinVar RCV Id: RCV004524658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Thr92Ser
CA376770466
NM_020630.6:c.274A>T
CA376770468
NM_020630.6:c.275C>G