Canonical Allele Identifier: PA658668147
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 486308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Ile669Val
CA036871
NM_020975.6:c.2005A>G