Canonical Allele Identifier: PA2828048368
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 2640418
ClinVar RCV Id: RCV003417332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Arg563Leu
CA376556211
NM_001355216.1:c.1688G>T