Canonical Allele Identifier: PA2828048568
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 665292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Ala612Thr
CA376556801
NM_001355216.1:c.1834G>A