Canonical Allele Identifier: PA2828048536
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Ile598Met
CA008919
NM_001355216.1:c.1794C>G