Canonical Allele Identifier: PA169095
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 142676

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Arg833His
CA008821
NM_020975.6:c.2498G>A