Canonical Allele Identifier: PA2828048581
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 3227536
ClinVar RCV Id: RCV004524654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Met614Arg
CA376556839
NM_001355216.1:c.1841T>G