Canonical Allele Identifier: PA2828048061
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 187701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Thr488Met
CA008602
NM_001355216.1:c.1463C>T