Canonical Allele Identifier: PA916043071
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Arg76Gln
CA009415
NM_001355216.1:c.227G>A