Canonical Allele Identifier: PA2828048327
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 659223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Lys554Thr
CA039164
NM_001355216.1:c.1661A>C