Canonical Allele Identifier: PA2828048572
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 3227535
ClinVar RCV Id: RCV004524653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Glu613Ala
CA376556815
NM_001355216.1:c.1838A>C