Canonical Allele Identifier: PA916043077
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 38594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Thr84Ile
CA007399
NM_001355216.1:c.251C>T