Canonical Allele Identifier: PA658670202
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 486342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Gly23Asp
CA376768119
NM_020975.6:c.68G>A