Canonical Allele Identifier: PA2828048912
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 405522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Glu724Lys
CA041492
NM_001355216.1:c.2170G>A