Canonical Allele Identifier: PA2828048544
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1800643
ClinVar RCV Id: RCV002461782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Trp602Ser
CA376556630
NM_001355216.1:c.1805G>C