Canonical Allele Identifier: PA891848076
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 568399
ClinVar RCV Id: RCV000688750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Glu805Gln
CA376556055
NM_020975.6:c.2413G>C