Canonical Allele Identifier: PA2829939397
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 486331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Arg99Trp
CA376770511
NM_020630.6:c.295C>T