Canonical Allele Identifier: PA2829939274
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 997535
ClinVar RCV Id: RCV001292753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Arg67Gly
CA376770298
NM_020630.6:c.199C>G