Canonical Allele Identifier: PA2828047984
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 372079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Val452Met
CA037364
NM_001355216.1:c.1354G>A