Canonical Allele Identifier: PA2829940000
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 477385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Thr244Ile
CA044641
NM_020630.6:c.731C>T