Canonical Allele Identifier: PA658670342
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 477391
ClinVar RCV Id: RCV000535337 RCV000679756 RCV002377189 RCV003459266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Thr315Pro
CA045562
NM_020975.6:c.943A>C