Canonical Allele Identifier: PA2829939074
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1448380
ClinVar RCV Id: RCV002012141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Pro20Leu
CA376768105
NM_020630.6:c.59C>T