Canonical Allele Identifier: PA128378
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24943
ClinVar RCV Id: RCV000148782 RCV000410539 RCV000411157 RCV000571277 RCV000799360 RCV002490401 RCV003460490
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Glu818Lys
CA008797
NM_020975.6:c.2452G>A