Canonical Allele Identifier: PA2828047814
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24932
ClinVar Variation Id: 230926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Lys412Asn
CA008525
NM_001355216.1:c.1236G>T
CA036775
NM_001355216.1:c.1236G>C