Canonical Allele Identifier: PA2829939410
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 941689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.His103Tyr
CA376770535
NM_020630.6:c.307C>T