Canonical Allele Identifier: PA332106
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 132762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Gly568Ser
CA007718
NM_020630.6:c.1702G>A