Canonical Allele Identifier: PA2829939373
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 2131000
ClinVar RCV Id: RCV003047985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Gly93Asp
CA376770474
NM_020630.6:c.278G>A