Canonical Allele Identifier: PA2828048550
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 2868475
ClinVar RCV Id: RCV003646756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Ile604Thr
CA376556672
NM_001355216.1:c.1811T>C