Canonical Allele Identifier: PA2828048433
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 3074327
ClinVar RCV Id: RCV004012869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Asn580Thr
CA206266614
NM_001355216.1:c.1739A>C