Canonical Allele Identifier: PA128107
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Gly321Arg
CA009403
NM_020630.6:c.961G>A
CA376546111
NM_020630.6:c.961G>C