Canonical Allele Identifier: PA2829941946
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 936959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Pro766Leu
CA206264383
NM_020630.6:c.2297C>T