Canonical Allele Identifier: PA2829939252
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 2701823
ClinVar RCV Id: RCV003533984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Glu62Asp
CA376770269
NM_020630.6:c.186G>C
CA376770270
NM_020630.6:c.186G>T