Canonical Allele Identifier: PA658668204
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 477346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Ala793Val
CA376555898
NM_020975.6:c.2378C>T