Canonical Allele Identifier: PA2829939260
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1781872
ClinVar RCV Id: RCV002415289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Val63Leu
CA036079
NM_020630.6:c.187G>T
CA376770272
NM_020630.6:c.187G>C