Canonical Allele Identifier: PA2828047327
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 132762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Gly314Ser
CA007718
NM_001355216.1:c.940G>A