Canonical Allele Identifier: PA128326
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24932
ClinVar Variation Id: 230926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Lys666Asn
CA008525
NM_020975.6:c.1998G>T
CA036775
NM_020975.6:c.1998G>C