Canonical Allele Identifier: PA2828048379
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 3075551
ClinVar RCV Id: RCV004017069
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Glu564Gln
CA376556218
NM_001355216.1:c.1690G>C