Canonical Allele Identifier: PA2580441043
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1729813
ClinVar RCV Id: RCV002445810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Ser110Arg
CA376770583
NM_020975.6:c.328A>C
CA376770588
NM_020975.6:c.330T>A
CA376770589
NM_020975.6:c.330T>G