Canonical Allele Identifier: PA2829938951
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1771753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Thr5Ala
CA376768019
NM_020630.6:c.13A>G