Canonical Allele Identifier: PA306735
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 201136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Ala1105Val
CA010953
NM_020975.6:c.3314C>T