Canonical Allele Identifier: PA2828048128
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 486317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Ala510Thr
CA038434
NM_001355216.1:c.1528G>A