Canonical Allele Identifier: PA106468
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1069381
ClinVar RCV Id: RCV001381227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Arg77Cys
CA376770362
NM_020975.6:c.229C>T