Canonical Allele Identifier: PA2829942097
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1481838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Ser819Arg
CA376556228
NM_020630.6:c.2455A>C
CA376556240
NM_020630.6:c.2457C>A
CA376556242
NM_020630.6:c.2457C>G