Canonical Allele Identifier: PA2828047522
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Cys364Gly
CA007995
NM_001355216.1:c.1090T>G