Canonical Allele Identifier: PA2829942227
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 665292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Ala866Thr
CA376556801
NM_020630.6:c.2596G>A