Canonical Allele Identifier: PA130242
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 38594
ClinVar RCV Id: RCV000570795 RCV000709106 RCV001046577 RCV001262456
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Thr338Ile
CA007399
NM_020630.6:c.1013C>T