Canonical Allele Identifier: PA2828048024
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 136108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Lys468Asn
CA008592
NM_001355216.1:c.1404G>T
CA376554271
NM_001355216.1:c.1404G>C