Canonical Allele Identifier: PA916054983
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 821031
ClinVar Variation Id: 1509387
ClinVar RCV Id: RCV002017866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Glu762Asp
CA376555521
NM_020975.6:c.2286G>C
CA376555523
NM_020975.6:c.2286G>T