Canonical Allele Identifier: PA2829942041
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 568399
ClinVar RCV Id: RCV000688750

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Glu805Gln
CA376556055
NM_020630.6:c.2413G>C