Canonical Allele Identifier: PA2828048000
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 580338
ClinVar RCV Id: RCV000703840 RCV000709118 RCV000708756 RCV001104665 RCV001104666 RCV001104667 RCV001104668 RCV002499266
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Lys456Arg
CA037409
NM_001355216.1:c.1367A>G