Canonical Allele Identifier: PA645450370
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 423618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Pro20dup
CA16618957
NM_020975.6:c.59_61dup