Canonical Allele Identifier: PA198348
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 187701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Thr742Met
CA008602
NM_020975.6:c.2225C>T