Canonical Allele Identifier: PA658668177
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 486317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Ala764Thr
CA038434
NM_020975.6:c.2290G>A