Canonical Allele Identifier: PA2829940081
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 543748

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Asp266Asn
CA376545111
NM_020630.6:c.796G>A