Canonical Allele Identifier: PA2829940277
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 477391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Thr315Pro
CA045562
NM_020630.6:c.943A>C