Canonical Allele Identifier: PA106877
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Cys634Tyr
CA008348
NM_020975.6:c.1901G>A