Canonical Allele Identifier: PA2828048688
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1364129
ClinVar RCV Id: RCV001937357

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Glu648Ala
CA376557266
NM_001355216.1:c.1943A>C