Canonical Allele Identifier: PA2829942233
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1002688
ClinVar RCV Id: RCV001299149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Met868Ile
CA376556841
NM_020630.6:c.2604G>A
CA376556842
NM_020630.6:c.2604G>C
CA376556844
NM_020630.6:c.2604G>T