Canonical Allele Identifier: PA2828047824
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 486308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Ile415Val
CA036871
NM_001355216.1:c.1243A>G