Canonical Allele Identifier: PA2829939087
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1755516
ClinVar RCV Id: RCV002369484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Gly23Arg
CA376768117
NM_020630.6:c.67G>C