Canonical Allele Identifier: PA2828048414
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 232162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Ser575Gly
CA039406
NM_001355216.1:c.1723A>G