Canonical Allele Identifier: PA2828047440
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 477327

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Arg346Trp
CA035694
NM_001355216.1:c.1036C>T