Canonical Allele Identifier: PA2829942613
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 241356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Thr1038Ile
CA042623
NM_020630.6:c.3113C>T