Canonical Allele Identifier: PA2828048234
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1479171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Tyr537Cys
CA376555872
NM_001355216.1:c.1610A>G