Canonical Allele Identifier: PA2829939173
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 818716
ClinVar RCV Id: RCV001010592 RCV003532346
ClinVar Variation Id: 1951525
ClinVar RCV Id: RCV002686228 RCV003375669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Asp43Glu
CA376770156
NM_020630.6:c.129C>A
CA376770157
NM_020630.6:c.129C>G