Canonical Allele Identifier: PA645451188
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 372080

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Leu1048Val
CA042766
NM_020975.6:c.3142C>G